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esv2421641

  • Variant Calls:35
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,109

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 172 SVs from 49 studies. See in: genome view    
Remapped(Score: Perfect):34,859,623-34,871,731Question Mark
Overlapping variant regions from other studies: 172 SVs from 49 studies. See in: genome view    
Remapped(Score: Perfect):34,899,235-34,911,343Question Mark
Overlapping variant regions from other studies: 43 SVs from 18 studies. See in: genome view    
Submitted genomic34,865,760-34,877,868Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2421641RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr734,859,62334,871,731
esv2421641RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr734,899,23534,911,343
esv2421641Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000007.12Chr734,865,76034,877,868

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
essv5003409deletionNA19099SNP arraySNP genotyping analysis1148
essv5004295deletionNA18510SNP arraySNP genotyping analysis1141
essv5016882deletionNA19467SNP arraySNP genotyping analysis1150
essv5020085deletionNA19176SNP arraySNP genotyping analysis1162
essv5020091deletionNA19123SNP arraySNP genotyping analysis1143
essv5024228deletionNA21318SNP arraySNP genotyping analysis1118
essv5029916deletionNA19103SNP arraySNP genotyping analysis1143
essv5033340deletionNA19161SNP arraySNP genotyping analysis1155
essv5034044deletionNA19834SNP arraySNP genotyping analysis1144
essv5034154deletionNA19223SNP arraySNP genotyping analysis1144
essv5052543deletionNA19399SNP arraySNP genotyping analysis1143
essv5053245deletionNA19160SNP arraySNP genotyping analysis1147
essv5058885deletionNA19211SNP arraySNP genotyping analysis1143
essv5060881deletionNA20356SNP arraySNP genotyping analysis1150
essv5061924deletionNA21678SNP arraySNP genotyping analysis1129
essv5062576deletionNA21636SNP arraySNP genotyping analysis1134
essv5064262deletionNA19210SNP arraySNP genotyping analysis1149
essv5065134deletionNA19327SNP arraySNP genotyping analysis1151
essv5065597deletionNA19836SNP arraySNP genotyping analysis0140
essv5072426deletionNA19101SNP arraySNP genotyping analysis1141
essv5077003deletionNA19122SNP arraySNP genotyping analysis1151
essv5084793deletionNA18498SNP arraySNP genotyping analysis1156
essv5092827deletionNA19221SNP arraySNP genotyping analysis1148
essv5092843deletionNA19108SNP arraySNP genotyping analysis1154
essv5099940deletionNA19173SNP arraySNP genotyping analysis1135
essv5105087deletionNA19189SNP arraySNP genotyping analysis1130
essv5105610deletionNA19171SNP arraySNP genotyping analysis1148
essv5117022deletionNA19191SNP arraySNP genotyping analysis1162
essv5120279deletionNA21635SNP arraySNP genotyping analysis1124
essv5122520deletionNA19185SNP arraySNP genotyping analysis1137
essv5136435deletionNA18923SNP arraySNP genotyping analysis1135
essv5136988deletionNA19835SNP arraySNP genotyping analysis1135
essv5141243deletionNA20358SNP arraySNP genotyping analysis1150
essv5153066deletionNA18910SNP arraySNP genotyping analysis1154
essv5158930deletionNA19182SNP arraySNP genotyping analysis1148

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv5003409RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5004295RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5016882RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5020085RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5020091RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5024228RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5029916RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5033340RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5034044RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5034154RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5052543RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5053245RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5058885RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5060881RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5061924RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5062576RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5064262RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5065134RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5065597RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5072426RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5077003RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5084793RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5092827RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5092843RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5099940RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5105087RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5105610RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5117022RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5120279RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5122520RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5136435RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5136988RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5141243RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5153066RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5158930RemappedPerfectNC_000007.14:g.(?_
34859623)_(3487173
1_?)del
GRCh38.p12First PassNC_000007.14Chr734,859,62334,871,731
essv5003409RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5004295RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5016882RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5020085RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5020091RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5024228RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5029916RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5033340RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5034044RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5034154RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5052543RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5053245RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5058885RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5060881RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5061924RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5062576RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5064262RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5065134RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5065597RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5072426RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5077003RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5084793RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5092827RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5092843RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5099940RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5105087RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5105610RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5117022RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5120279RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5122520RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5136435RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5136988RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5141243RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5153066RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5158930RemappedPerfectNC_000007.13:g.(?_
34899235)_(3491134
3_?)del
GRCh37.p13First PassNC_000007.13Chr734,899,23534,911,343
essv5003409Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5004295Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5016882Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5020085Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5020091Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5024228Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5029916Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5033340Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5034044Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5034154Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5052543Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5053245Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5058885Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5060881Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5061924Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5062576Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5064262Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5065134Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5065597Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5072426Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5077003Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5084793Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5092827Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5092843Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5099940Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5105087Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5105610Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5117022Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5120279Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
essv5122520Submitted genomicNC_000007.12:g.(?_
34865760)_(3487786
8_?)del
NCBI36 (hg18)NC_000007.12Chr734,865,76034,877,868
Showing 100 of 105

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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