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nsv6691650

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,427

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 108 SVs from 28 studies. See in: genome view    
    Submitted genomic88,049,610-88,051,036Question Mark
    Overlapping variant regions from other studies: 110 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):88,349,129-88,350,555Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6691650Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr288,049,61088,051,036
    nsv6691650RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr288,349,12988,350,555

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18469762deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18469762Submitted genomicNC_000002.12:g.880
    49610_88051036del
    GRCh38 (hg38)NC_000002.12Chr288,049,61088,051,036
    nssv18469762RemappedPerfectNC_000002.11:g.883
    49129_88350555del
    GRCh37.p13First PassNC_000002.11Chr288,349,12988,350,555

    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)
    nssv184697624e-061274630
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