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esv2761883

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:22,711

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 332 SVs from 49 studies. See in: genome view    
Remapped(Score: Perfect):93,598,378-93,621,088Question Mark
Overlapping variant regions from other studies: 332 SVs from 49 studies. See in: genome view    
Remapped(Score: Perfect):94,141,607-94,164,317Question Mark
Overlapping variant regions from other studies: 147 SVs from 16 studies. See in: genome view    
Submitted genomic91,942,611-91,965,321Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2761883RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000015.10Chr1593,598,37893,621,088
esv2761883RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1594,141,60794,164,317
esv2761883Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000015.8Chr1591,942,61191,965,321

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv7000418copy number lossSW_1000SNP arraySNP genotyping analysis42

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv7000418RemappedPerfectNC_000015.10:g.(?_
93598378)_(9362108
8_?)del
GRCh38.p12First PassNC_000015.10Chr1593,598,37893,621,088
essv7000418RemappedPerfectNC_000015.9:g.(?_9
4141607)_(94164317
_?)del
GRCh37.p13First PassNC_000015.9Chr1594,141,60794,164,317
essv7000418Submitted genomicNC_000015.8:g.(?_9
1942611)_(91965321
_?)del
NCBI36 (hg18)NC_000015.8Chr1591,942,61191,965,321

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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