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esv2479396

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:45,785

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 593 SVs from 67 studies. See in: genome view    
Remapped(Score: Perfect):21,526,741-21,572,525Question Mark
Overlapping variant regions from other studies: 621 SVs from 67 studies. See in: genome view    
Remapped(Score: Perfect):21,526,850-21,572,634Question Mark
Overlapping variant regions from other studies: 270 SVs from 15 studies. See in: genome view    
Submitted genomic21,562,607-21,608,391Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2479396RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr521,526,74121,572,525
esv2479396RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr521,526,85021,572,634
esv2479396Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000005.8Chr521,562,60721,608,391

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5394127copy number gainNA18507SequencingRead depth232,775

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv5394127RemappedPerfectNC_000005.10:g.(?_
21526741)_(2157252
5_?)dup
GRCh38.p12First PassNC_000005.10Chr521,526,74121,572,525
essv5394127RemappedPerfectNC_000005.9:g.(?_2
1526850)_(21572634
_?)dup
GRCh37.p13First PassNC_000005.9Chr521,526,85021,572,634
essv5394127Submitted genomicNC_000005.8:g.(?_2
1562607)_(21608391
_?)dup
NCBI36 (hg18)NC_000005.8Chr521,562,60721,608,391

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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