U.S. flag

An official website of the United States government

nsv6407401

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:605,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2081 SVs from 97 studies. See in: genome view    
    Submitted genomic140,339,301-140,944,600Question Mark
    Overlapping variant regions from other studies: 989 SVs from 70 studies. See in: genome view    
    Remapped(Score: Pass):139,718,886-140,144,409Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6407401Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5140,339,301140,944,600
    nsv6407401RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5139,718,886140,144,409

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18215082duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18215082Submitted genomicNC_000005.10:g.140
    339301_140944600du
    p
    GRCh38 (hg38)NC_000005.10Chr5140,339,301140,944,600
    nssv18215082RemappedPassNC_000005.9:g.1397
    18886_140144409dup
    GRCh37.p13First PassNC_000005.9Chr5139,718,886140,144,409

    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)
    nssv18215082<0.001834222
    Support Center