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nsv6187987

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 119 SVs from 16 studies. See in: genome view    
Submitted genomic66,224,656-66,224,720Question Mark
Overlapping variant regions from other studies: 119 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):64,220,774-64,220,838Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6187987Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1766,224,65666,224,720
nsv6187987RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1764,220,77464,220,838

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17935038deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17935038Submitted genomicNC_000017.11:g.662
24656_66224720del
GRCh38 (hg38)NC_000017.11Chr1766,224,65666,224,720
nssv17935038RemappedPerfectNC_000017.10:g.642
20774_64220838del
GRCh37.p13First PassNC_000017.10Chr1764,220,77464,220,838

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)
nssv17935038<0.00111010
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