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nsv6376737

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:264,431

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 697 SVs from 61 studies. See in: genome view    
    Submitted genomic99,180,425-99,444,855Question Mark
    Overlapping variant regions from other studies: 697 SVs from 61 studies. See in: genome view    
    Remapped(Score: Perfect):100,101,582-100,366,012Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6376737Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr499,180,42599,444,855
    nsv6376737RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4100,101,582100,366,012

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18214410duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18214410Submitted genomicNC_000004.12:g.991
    80425_99444855dup
    GRCh38 (hg38)NC_000004.12Chr499,180,42599,444,855
    nssv18214410RemappedPerfectNC_000004.11:g.100
    101582_100366012du
    p
    GRCh37.p13First PassNC_000004.11Chr4100,101,582100,366,012

    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)
    nssv18214410<0.001139302
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