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nsv6410875

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:43,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 254 SVs from 53 studies. See in: genome view    
    Submitted genomic140,690,101-140,733,400Question Mark
    Overlapping variant regions from other studies: 250 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):140,069,686-140,112,985Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6410875Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5140,690,101140,733,400
    nsv6410875RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5140,069,686140,112,985

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18215087duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18215087Submitted genomicNC_000005.10:g.140
    690101_140733400du
    p
    GRCh38 (hg38)NC_000005.10Chr5140,690,101140,733,400
    nssv18215087RemappedPerfectNC_000005.9:g.1400
    69686_140112985dup
    GRCh37.p13First PassNC_000005.9Chr5140,069,686140,112,985

    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)
    nssv18215087<0.001135120
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