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nsv6755982

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,716

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 145 SVs from 38 studies. See in: genome view    
    Submitted genomic75,546,847-75,554,562Question Mark
    Overlapping variant regions from other studies: 145 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):76,472,057-76,479,772Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6755982Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr475,546,84775,554,562
    nsv6755982RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr476,472,05776,479,772

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18500430deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18500430Submitted genomicNC_000004.12:g.755
    46847_75554562del
    GRCh38 (hg38)NC_000004.12Chr475,546,84775,554,562
    nssv18500430RemappedPerfectNC_000004.11:g.764
    72057_76479772del
    GRCh37.p13First PassNC_000004.11Chr476,472,05776,479,772

    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)
    nssv185004304e-061276194
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