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nsv6616315

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:768

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 120 SVs from 24 studies. See in: genome view    
    Submitted genomic109,438,735-109,439,502Question Mark
    Overlapping variant regions from other studies: 120 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):109,759,938-109,760,705Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6616315Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6109,438,735109,439,502
    nsv6616315RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6109,759,938109,760,705

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18136624deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18136624Submitted genomicNC_000006.12:g.109
    438735_109439502de
    l
    GRCh38 (hg38)NC_000006.12Chr6109,438,735109,439,502
    nssv18136624RemappedPerfectNC_000006.11:g.109
    759938_109760705de
    l
    GRCh37.p13First PassNC_000006.11Chr6109,759,938109,760,705

    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)
    nssv18136624<0.001132954
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