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nsv6817868

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:261,030

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 868 SVs from 70 studies. See in: genome view    
    Submitted genomic118,438,498-118,699,527Question Mark
    Overlapping variant regions from other studies: 868 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):118,759,661-119,020,690Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6817868Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6118,438,498118,699,527
    nsv6817868RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6118,759,661119,020,690

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18705650duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18705650Submitted genomicNC_000006.12:g.118
    438498_118699527du
    p
    GRCh38 (hg38)NC_000006.12Chr6118,438,498118,699,527
    nssv18705650RemappedPerfectNC_000006.11:g.118
    759661_119020690du
    p
    GRCh37.p13First PassNC_000006.11Chr6118,759,661119,020,690

    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)
    nssv187056504e-061275894
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