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nsv5524833

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:148,817

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 592 SVs from 65 studies. See in: genome view    
Submitted genomic11,804,226-11,953,042Question Mark
Overlapping variant regions from other studies: 592 SVs from 65 studies. See in: genome view    
Remapped(Score: Perfect):11,915,041-12,063,857Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5524833Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1911,804,22611,953,042
nsv5524833RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1911,915,04112,063,857

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17721443duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17721443Submitted genomicNC_000019.10:g.118
04226_11953042dup
GRCh38 (hg38)NC_000019.10Chr1911,804,22611,953,042
nssv17721443RemappedPerfectNC_000019.9:g.1191
5041_12063857dup
GRCh37.p13First PassNC_000019.9Chr1911,915,04112,063,857

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17721443<0.00116404
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