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nsv6769045

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,232

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 118 SVs from 23 studies. See in: genome view    
    Submitted genomic96,668,779-96,672,010Question Mark
    Overlapping variant regions from other studies: 118 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):96,004,483-96,007,714Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6769045Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr596,668,77996,672,010
    nsv6769045RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr596,004,48396,007,714

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18518022deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18518022Submitted genomicNC_000005.10:g.966
    68779_96672010del
    GRCh38 (hg38)NC_000005.10Chr596,668,77996,672,010
    nssv18518022RemappedPerfectNC_000005.9:g.9600
    4483_96007714del
    GRCh37.p13First PassNC_000005.9Chr596,004,48396,007,714

    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)
    nssv185180227e-062275906
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