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nsv6396816

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,455

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 124 SVs from 33 studies. See in: genome view    
    Submitted genomic163,443,060-163,455,514Question Mark
    Overlapping variant regions from other studies: 124 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):162,870,066-162,882,520Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6396816Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5163,443,060163,455,514
    nsv6396816RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5162,870,066162,882,520

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18215962duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18215962Submitted genomicNC_000005.10:g.163
    443060_163455514du
    p
    GRCh38 (hg38)NC_000005.10Chr5163,443,060163,455,514
    nssv18215962RemappedPerfectNC_000005.9:g.1628
    70066_162882520dup
    GRCh37.p13First PassNC_000005.9Chr5162,870,066162,882,520

    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)
    nssv18215962<0.001139212
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