U.S. flag

An official website of the United States government

nsv7035035

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:239,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 756 SVs from 65 studies. See in: genome view    
    Submitted genomic37,242,001-37,481,000Question Mark
    Overlapping variant regions from other studies: 756 SVs from 65 studies. See in: genome view    
    Remapped(Score: Perfect):35,870,404-36,109,402Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7035035Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2037,242,00137,481,000
    nsv7035035RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2035,870,40436,109,402

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18644237duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18644237Submitted genomicNC_000020.11:g.372
    42001_37481000dup
    GRCh38 (hg38)NC_000020.11Chr2037,242,00137,481,000
    nssv18644237RemappedPerfectNC_000020.10:g.358
    70404_36109402dup
    GRCh37.p13First PassNC_000020.10Chr2035,870,40436,109,402

    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)
    nssv186442375e-0514272250
    Support Center