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nsv6573818

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,354,656

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 19894 SVs from 124 studies. See in: genome view    
    Submitted genomic153,431,058-160,785,713Question Mark
    Overlapping variant regions from other studies: 19896 SVs from 124 studies. See in: genome view    
    Remapped(Score: Good):153,752,193-161,206,745Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6573818Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6153,431,058160,785,713
    nsv6573818RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6153,752,193161,206,745

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18270036inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18270036Submitted genomicNC_000006.12:g.153
    431058_160785713in
    v
    GRCh38 (hg38)NC_000006.12Chr6153,431,058160,785,713
    nssv18270036RemappedGoodNC_000006.11:g.153
    752193_161206745in
    v
    GRCh37.p13First PassNC_000006.11Chr6153,752,193161,206,745

    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)
    nssv182700360.288878730464
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