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nsv4575464

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 64 SVs from 8 studies. See in: genome view    
Remapped(Score: Perfect):67,003,590-67,003,590Question Mark
Overlapping variant regions from other studies: 64 SVs from 8 studies. See in: genome view    
Submitted genomic67,037,493-67,037,493Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4575464RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1667,003,59067,003,590
nsv4575464Submitted genomicGRCh37.p13Primary AssemblyNC_000016.9Chr1667,037,49367,037,493

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16013002sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16013002RemappedPerfectNC_000016.10:g.670
03590_67003591ins1
240
GRCh38.p12First PassNC_000016.10Chr1667,003,59067,003,590
nssv16013002Submitted genomicNC_000016.9:g.6703
7493_67037494ins12
40
GRCh37.p13NC_000016.9Chr1667,037,49367,037,493

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)
nssv16013002<0.001421694
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