U.S. flag

An official website of the United States government

nsv6897972

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:173

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 103 SVs from 24 studies. See in: genome view    
    Submitted genomic75,826,771-75,826,943Question Mark
    Overlapping variant regions from other studies: 103 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):77,586,529-77,586,701Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6897972Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1075,826,77175,826,943
    nsv6897972RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1077,586,52977,586,701

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18583908duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18583908Submitted genomicNC_000010.11:g.758
    26771_75826943dup
    GRCh38 (hg38)NC_000010.11Chr1075,826,77175,826,943
    nssv18583908RemappedPerfectNC_000010.10:g.775
    86529_77586701dup
    GRCh37.p13First PassNC_000010.10Chr1077,586,52977,586,701

    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)
    nssv185839084e-061231816
    Support Center