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nsv6411582

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,813

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 100 SVs from 23 studies. See in: genome view    
    Submitted genomic57,003,944-57,008,756Question Mark
    Overlapping variant regions from other studies: 100 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):56,868,742-56,873,554Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6411582Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr657,003,94457,008,756
    nsv6411582RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr656,868,74256,873,554

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18146578deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18146578Submitted genomicNC_000006.12:g.570
    03944_57008756del
    GRCh38 (hg38)NC_000006.12Chr657,003,94457,008,756
    nssv18146578RemappedPerfectNC_000006.11:g.568
    68742_56873554del
    GRCh37.p13First PassNC_000006.11Chr656,868,74256,873,554

    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)
    nssv18146578<0.001139196
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