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esv2421333

  • Variant Calls:29
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,381

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 196 SVs from 57 studies. See in: genome view    
Remapped(Score: Perfect):60,048,702-60,063,082Question Mark
Overlapping variant regions from other studies: 196 SVs from 57 studies. See in: genome view    
Remapped(Score: Perfect):60,082,606-60,096,986Question Mark
Overlapping variant regions from other studies: 63 SVs from 18 studies. See in: genome view    
Submitted genomic58,640,107-58,654,487Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2421333RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1660,048,70260,063,082
esv2421333RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1660,082,60660,096,986
esv2421333Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000016.8Chr1658,640,10758,654,487

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
essv5002042deletionNA19064SNP arraySNP genotyping analysis1129
essv5004894deletionNA19784SNP arraySNP genotyping analysis1141
essv5006633deletionNA19776SNP arraySNP genotyping analysis1133
essv5007951deletionNA19625SNP arraySNP genotyping analysis1175
essv5014065deletionNA18757SNP arraySNP genotyping analysis1141
essv5016211deletionNA18117SNP arraySNP genotyping analysis1124
essv5017407deletionNA18643SNP arraySNP genotyping analysis1145
essv5018583deletionNA18552SNP arraySNP genotyping analysis1143
essv5021224deletionNA19086SNP arraySNP genotyping analysis1128
essv5026503deletionNA18544SNP arraySNP genotyping analysis1131
essv5026566deletionNA19720SNP arraySNP genotyping analysis1125
essv5039785deletionNA19772SNP arraySNP genotyping analysis1131
essv5040030deletionNA19770SNP arraySNP genotyping analysis1126
essv5047550deletionNA18619SNP arraySNP genotyping analysis1131
essv5068493deletionNA19783SNP arraySNP genotyping analysis1133
essv5069357deletionNA19782SNP arraySNP genotyping analysis1130
essv5070050deletionNA19055SNP arraySNP genotyping analysis1129
essv5083701deletionNA20887SNP arraySNP genotyping analysis1139
essv5087154deletionNA18965SNP arraySNP genotyping analysis1129
essv5089571deletionNA18529SNP arraySNP genotyping analysis1124
essv5109511deletionNA18118SNP arraySNP genotyping analysis1133
essv5111734deletionNA18120SNP arraySNP genotyping analysis1121
essv5112220deletionNA18133SNP arraySNP genotyping analysis1118
essv5113209deletionNA19778SNP arraySNP genotyping analysis1125
essv5128180deletionNA17977SNP arraySNP genotyping analysis1123
essv5132332deletionNA19716SNP arraySNP genotyping analysis1133
essv5142474deletionNA17998SNP arraySNP genotyping analysis1120
essv5142530deletionNA18969SNP arraySNP genotyping analysis1139
essv5152488deletionNA19721SNP arraySNP genotyping analysis1122

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv5002042RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5004894RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5006633RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5007951RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5014065RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5016211RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5017407RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5018583RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5021224RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5026503RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5026566RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5039785RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5040030RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5047550RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5068493RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5069357RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5070050RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5083701RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5087154RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5089571RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5109511RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5111734RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5112220RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5113209RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5128180RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5132332RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5142474RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5142530RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5152488RemappedPerfectNC_000016.10:g.(?_
60048702)_(6006308
2_?)del
GRCh38.p12First PassNC_000016.10Chr1660,048,70260,063,082
essv5002042RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5004894RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5006633RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5007951RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5014065RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5016211RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5017407RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5018583RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5021224RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5026503RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5026566RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5039785RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5040030RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5047550RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5068493RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5069357RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5070050RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5083701RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5087154RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5089571RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5109511RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5111734RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5112220RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5113209RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5128180RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5132332RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5142474RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5142530RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5152488RemappedPerfectNC_000016.9:g.(?_6
0082606)_(60096986
_?)del
GRCh37.p13First PassNC_000016.9Chr1660,082,60660,096,986
essv5002042Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5004894Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5006633Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5007951Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5014065Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5016211Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5017407Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5018583Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5021224Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5026503Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5026566Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5039785Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5040030Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5047550Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5068493Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5069357Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5070050Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5083701Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5087154Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5089571Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5109511Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5111734Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5112220Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5113209Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5128180Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5132332Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5142474Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5142530Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487
essv5152488Submitted genomicNC_000016.8:g.(?_5
8640107)_(58654487
_?)del
NCBI36 (hg18)NC_000016.8Chr1658,640,10758,654,487

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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