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nsv6739948

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,656

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 176 SVs from 35 studies. See in: genome view    
    Submitted genomic164,773,450-164,779,105Question Mark
    Overlapping variant regions from other studies: 176 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):165,694,602-165,700,257Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6739948Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4164,773,450164,779,105
    nsv6739948RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4165,694,602165,700,257

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18494183deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18494183Submitted genomicNC_000004.12:g.164
    773450_164779105de
    l
    GRCh38 (hg38)NC_000004.12Chr4164,773,450164,779,105
    nssv18494183RemappedPerfectNC_000004.11:g.165
    694602_165700257de
    l
    GRCh37.p13First PassNC_000004.11Chr4165,694,602165,700,257

    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)
    nssv18494183<0.00132275416
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