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esv2761895

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26,794

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 286 SVs from 44 studies. See in: genome view    
Remapped(Score: Perfect):6,527,388-6,554,181Question Mark
Overlapping variant regions from other studies: 286 SVs from 44 studies. See in: genome view    
Remapped(Score: Perfect):6,577,389-6,604,182Question Mark
Overlapping variant regions from other studies: 99 SVs from 15 studies. See in: genome view    
Submitted genomic6,517,390-6,544,183Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2761895RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr166,527,3886,554,181
esv2761895RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr166,577,3896,604,182
esv2761895Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000016.8Chr166,517,3906,544,183

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv7000509copy number lossSW_1000SNP arraySNP genotyping analysis42

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv7000509RemappedPerfectNC_000016.10:g.(?_
6527388)_(6554181_
?)del
GRCh38.p12First PassNC_000016.10Chr166,527,3886,554,181
essv7000509RemappedPerfectNC_000016.9:g.(?_6
577389)_(6604182_?
)del
GRCh37.p13First PassNC_000016.9Chr166,577,3896,604,182
essv7000509Submitted genomicNC_000016.8:g.(?_6
517390)_(6544183_?
)del
NCBI36 (hg18)NC_000016.8Chr166,517,3906,544,183

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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