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nsv6609585

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,485

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 91 SVs from 26 studies. See in: genome view    
    Submitted genomic35,146,500-35,148,984Question Mark
    Overlapping variant regions from other studies: 91 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):35,186,112-35,188,596Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6609585Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr735,146,50035,148,984
    nsv6609585RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr735,186,11235,188,596

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18153104deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18153104Submitted genomicNC_000007.14:g.351
    46500_35148984del
    GRCh38 (hg38)NC_000007.14Chr735,146,50035,148,984
    nssv18153104RemappedPerfectNC_000007.13:g.351
    86112_35188596del
    GRCh37.p13First PassNC_000007.13Chr735,186,11235,188,596

    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)
    nssv18153104<0.001339260
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