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nsv6399064

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:341,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2536 SVs from 109 studies. See in: genome view    
    Submitted genomic180,956,101-181,297,100Question Mark
    Overlapping variant regions from other studies: 2537 SVs from 109 studies. See in: genome view    
    Remapped(Score: Perfect):180,383,101-180,724,101Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6399064Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5180,956,101181,297,100
    nsv6399064RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5180,383,101180,724,101

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18215171duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18215171Submitted genomicNC_000005.10:g.180
    956101_181297100du
    p
    GRCh38 (hg38)NC_000005.10Chr5180,956,101181,297,100
    nssv18215171RemappedPerfectNC_000005.9:g.1803
    83101_180724101dup
    GRCh37.p13First PassNC_000005.9Chr5180,383,101180,724,101

    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)
    nssv18215171<0.0011935516
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