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nsv6608576

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:615

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 93 SVs from 18 studies. See in: genome view    
    Submitted genomic130,428,093-130,428,707Question Mark
    Overlapping variant regions from other studies: 93 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):130,749,238-130,749,852Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6608576Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6130,428,093130,428,707
    nsv6608576RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6130,749,238130,749,852

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18138457deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18138457Submitted genomicNC_000006.12:g.130
    428093_130428707de
    l
    GRCh38 (hg38)NC_000006.12Chr6130,428,093130,428,707
    nssv18138457RemappedPerfectNC_000006.11:g.130
    749238_130749852de
    l
    GRCh37.p13First PassNC_000006.11Chr6130,749,238130,749,852

    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)
    nssv18138457<0.001238780
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