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nsv6795649

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:85,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 440 SVs from 59 studies. See in: genome view    
    Submitted genomic180,111,501-180,197,100Question Mark
    Overlapping variant regions from other studies: 440 SVs from 59 studies. See in: genome view    
    Remapped(Score: Perfect):179,538,501-179,624,100Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6795649Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5180,111,501180,197,100
    nsv6795649RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5179,538,501179,624,100

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18702135duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18702135Submitted genomicNC_000005.10:g.180
    111501_180197100du
    p
    GRCh38 (hg38)NC_000005.10Chr5180,111,501180,197,100
    nssv18702135RemappedPerfectNC_000005.9:g.1795
    38501_179624100dup
    GRCh37.p13First PassNC_000005.9Chr5179,538,501179,624,100

    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)
    nssv187021352.5e-057273148
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