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nsv6807998

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:45,884

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 300 SVs from 52 studies. See in: genome view    
    Submitted genomic5,039,885-5,085,768Question Mark
    Overlapping variant regions from other studies: 300 SVs from 52 studies. See in: genome view    
    Remapped(Score: Perfect):5,079,516-5,125,399Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6807998Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr75,039,8855,085,768
    nsv6807998RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr75,079,5165,125,399

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18544732deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18544732Submitted genomicNC_000007.14:g.503
    9885_5085768del
    GRCh38 (hg38)NC_000007.14Chr75,039,8855,085,768
    nssv18544732RemappedPerfectNC_000007.13:g.507
    9516_5125399del
    GRCh37.p13First PassNC_000007.13Chr75,079,5165,125,399

    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)
    nssv185447327e-062276240
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