U.S. flag

An official website of the United States government

nsv7009060

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:54

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 320 SVs from 36 studies. See in: genome view    
    Submitted genomic1,233,932-1,233,985Question Mark
    Overlapping variant regions from other studies: 320 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):1,233,931-1,233,984Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7009060Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr191,233,9321,233,985
    nsv7009060RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr191,233,9311,233,984

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18421541deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18421541Submitted genomicNC_000019.10:g.123
    3932_1233985del
    GRCh38 (hg38)NC_000019.10Chr191,233,9321,233,985
    nssv18421541RemappedPerfectNC_000019.9:g.1233
    931_1233984del
    GRCh37.p13First PassNC_000019.9Chr191,233,9311,233,984

    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)
    nssv184215414.3e-0511250066
    Support Center