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nsv6563707

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,736,939

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 18880 SVs from 125 studies. See in: genome view    
    Submitted genomic125,606,968-134,343,906Question Mark
    Overlapping variant regions from other studies: 18880 SVs from 125 studies. See in: genome view    
    Remapped(Score: Perfect):125,928,114-134,665,044Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6563707Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6125,606,968134,343,906
    nsv6563707RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6125,928,114134,665,044

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18271170inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18271170Submitted genomicNC_000006.12:g.125
    606968_134343906in
    v
    GRCh38 (hg38)NC_000006.12Chr6125,606,968134,343,906
    nssv18271170RemappedPerfectNC_000006.11:g.125
    928114_134665044in
    v
    GRCh37.p13First PassNC_000006.11Chr6125,928,114134,665,044

    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)
    nssv18271170<0.0011038116
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