U.S. flag

An official website of the United States government

nsv6828632

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:466,240

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1549 SVs from 88 studies. See in: genome view    
    Submitted genomic63,989,553-64,455,792Question Mark
    Overlapping variant regions from other studies: 1557 SVs from 88 studies. See in: genome view    
    Remapped(Score: Perfect):63,449,931-63,916,170Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6828632Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr763,989,55364,455,792
    nsv6828632RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr763,449,93163,916,170

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18726519duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18726519Submitted genomicNC_000007.14:g.639
    89553_64455792dup
    GRCh38 (hg38)NC_000007.14Chr763,989,55364,455,792
    nssv18726519RemappedPerfectNC_000007.13:g.634
    49931_63916170dup
    GRCh37.p13First PassNC_000007.13Chr763,449,93163,916,170

    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)
    nssv187265194e-061273252
    Support Center