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nsv6165759

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:83

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 215 SVs from 52 studies. See in: genome view    
Submitted genomic108,374,852-108,374,934Question Mark
Overlapping variant regions from other studies: 216 SVs from 52 studies. See in: genome view    
Remapped(Score: Perfect):108,917,474-108,917,556Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6165759Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1108,374,852108,374,934
nsv6165759RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1108,917,474108,917,556

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17862164deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17862164Submitted genomicNC_000001.11:g.108
374852_108374934de
l
GRCh38 (hg38)NC_000001.11Chr1108,374,852108,374,934
nssv17862164RemappedPerfectNC_000001.10:g.108
917474_108917556de
l
GRCh37.p13First PassNC_000001.10Chr1108,917,474108,917,556

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)
nssv178621640.07439526
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