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  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,719

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 71 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):90,142,682-90,153,400Question Mark
Overlapping variant regions from other studies: 77 SVs from 25 studies. See in: genome view    
Submitted genomic90,209,090-90,219,808Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6306388RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1690,142,68290,153,400
nsv6306388Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000016.9Chr1690,209,09090,219,808

Variant Call Information

Variant Call IDTypeMethodAnalysis

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
GRCh38.p12First PassNC_000016.10Chr1690,142,68290,153,400
nssv17968562Submitted genomicNC_000016.9:g.9020
GRCh37 (hg19)NC_000016.9Chr1690,209,09090,219,808

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
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