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esv2761764

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65,089

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 358 SVs from 50 studies. See in: genome view    
Remapped(Score: Perfect):99,665,236-99,730,324Question Mark
Overlapping variant regions from other studies: 358 SVs from 50 studies. See in: genome view    
Remapped(Score: Perfect):100,059,014-100,124,102Question Mark
Overlapping variant regions from other studies: 89 SVs from 16 studies. See in: genome view    
Submitted genomic98,583,145-98,648,233Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2761764RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1299,665,23699,730,324
esv2761764RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12100,059,014100,124,102
esv2761764Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000012.10Chr1298,583,14598,648,233

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv6997563copy number lossSW_0379SNP arraySNP genotyping analysis43

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv6997563RemappedPerfectNC_000012.12:g.(?_
99665236)_(9973032
4_?)del
GRCh38.p12First PassNC_000012.12Chr1299,665,23699,730,324
essv6997563RemappedPerfectNC_000012.11:g.(?_
100059014)_(100124
102_?)del
GRCh37.p13First PassNC_000012.11Chr12100,059,014100,124,102
essv6997563Submitted genomicNC_000012.10:g.(?_
98583145)_(9864823
3_?)del
NCBI36 (hg18)NC_000012.10Chr1298,583,14598,648,233

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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