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nsv6617739

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:677

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 107 SVs from 19 studies. See in: genome view    
    Submitted genomic122,411,418-122,412,094Question Mark
    Overlapping variant regions from other studies: 107 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):122,732,563-122,733,239Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6617739Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6122,411,418122,412,094
    nsv6617739RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6122,732,563122,733,239

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18137371deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18137371Submitted genomicNC_000006.12:g.122
    411418_122412094de
    l
    GRCh38 (hg38)NC_000006.12Chr6122,411,418122,412,094
    nssv18137371RemappedPerfectNC_000006.11:g.122
    732563_122733239de
    l
    GRCh37.p13First PassNC_000006.11Chr6122,732,563122,733,239

    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)
    nssv18137371<0.0011037944
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