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nsv6604101

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:656

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 114 SVs from 19 studies. See in: genome view    
    Submitted genomic109,415,379-109,416,034Question Mark
    Overlapping variant regions from other studies: 114 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):109,736,582-109,737,237Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6604101Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6109,415,379109,416,034
    nsv6604101RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6109,736,582109,737,237

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18136622deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18136622Submitted genomicNC_000006.12:g.109
    415379_109416034de
    l
    GRCh38 (hg38)NC_000006.12Chr6109,415,379109,416,034
    nssv18136622RemappedPerfectNC_000006.11:g.109
    736582_109737237de
    l
    GRCh37.p13First PassNC_000006.11Chr6109,736,582109,737,237

    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)
    nssv18136622<0.001538416
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