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nsv5509709

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26,596

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 188 SVs from 40 studies. See in: genome view    
Submitted genomic92,116,508-92,143,103Question Mark
Overlapping variant regions from other studies: 188 SVs from 40 studies. See in: genome view    
Remapped(Score: Perfect):92,510,284-92,536,879Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5509709Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1292,116,50892,143,103
nsv5509709RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1292,510,28492,536,879

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17684084duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17684084Submitted genomicNC_000012.12:g.921
16508_92143103dup
GRCh38 (hg38)NC_000012.12Chr1292,116,50892,143,103
nssv17684084RemappedPerfectNC_000012.11:g.925
10284_92536879dup
GRCh37.p13First PassNC_000012.11Chr1292,510,28492,536,879

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)
nssv17684084<0.00136404
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