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nsv6614052

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,283

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 132 SVs from 43 studies. See in: genome view    
    Submitted genomic64,019,206-64,034,488Question Mark
    Overlapping variant regions from other studies: 140 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):63,479,584-63,494,866Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6614052Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr764,019,20664,034,488
    nsv6614052RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr763,479,58463,494,866

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18231453duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18231453Submitted genomicNC_000007.14:g.640
    19206_64034488dup
    GRCh38 (hg38)NC_000007.14Chr764,019,20664,034,488
    nssv18231453RemappedPerfectNC_000007.13:g.634
    79584_63494866dup
    GRCh37.p13First PassNC_000007.13Chr763,479,58463,494,866

    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)
    nssv18231453<0.0011639298
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