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nsv7039011

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,142,610

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 11681 SVs from 124 studies. See in: genome view    
    Submitted genomic163,643,496-167,786,105Question Mark
    Overlapping variant regions from other studies: 11491 SVs from 124 studies. See in: genome view    
    Remapped(Score: Good):164,064,528-168,186,785Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039011Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6163,643,496167,786,105
    nsv7039011RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6164,064,528168,186,785

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18777647inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18777647Submitted genomicNC_000006.12:g.163
    643496_167786105in
    v
    GRCh38 (hg38)NC_000006.12Chr6163,643,496167,786,105
    nssv18777647RemappedGoodNC_000006.11:g.164
    064528_168186785in
    v
    GRCh37.p13First PassNC_000006.11Chr6164,064,528168,186,785

    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)
    nssv187776474e-060276268
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