U.S. flag

An official website of the United States government

nsv6935594

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:192

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 128 SVs from 24 studies. See in: genome view    
    Submitted genomic9,932,412-9,932,603Question Mark
    Overlapping variant regions from other studies: 129 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):10,085,011-10,085,202Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6935594Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr129,932,4129,932,603
    nsv6935594RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1210,085,01110,085,202

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18599122duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18599122Submitted genomicNC_000012.12:g.993
    2412_9932603dup
    GRCh38 (hg38)NC_000012.12Chr129,932,4129,932,603
    nssv18599122RemappedPerfectNC_000012.11:g.100
    85011_10085202dup
    GRCh37.p13First PassNC_000012.11Chr1210,085,01110,085,202

    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)
    nssv185991224e-061234890
    Support Center