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nsv4271331

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,904

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 29 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):75,985,762-75,994,665Question Mark
Overlapping variant regions from other studies: 29 SVs from 6 studies. See in: genome view    
Submitted genomic73,981,843-73,990,746Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4271331RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1775,985,76275,994,665
nsv4271331Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1773,981,84373,990,746

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15837434deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15837434RemappedPerfectNC_000017.11:g.759
85762_75994665del
GRCh38.p12First PassNC_000017.11Chr1775,985,76275,994,665
nssv15837434Submitted genomicNC_000017.10:g.739
81843_73990746del
GRCh37.p13NC_000017.10Chr1773,981,84373,990,746

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)
nssv15837434<0.001218904
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