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nsv7017756

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:274,188

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 894 SVs from 66 studies. See in: genome view    
    Submitted genomic37,548,077-37,822,264Question Mark
    Overlapping variant regions from other studies: 890 SVs from 66 studies. See in: genome view    
    Remapped(Score: Good):38,038,979-38,312,904Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7017756Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1937,548,07737,822,264
    nsv7017756RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1938,038,97938,312,904

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18423570deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18423570Submitted genomicNC_000019.10:g.375
    48077_37822264del
    GRCh38 (hg38)NC_000019.10Chr1937,548,07737,822,264
    nssv18423570RemappedGoodNC_000019.9:g.3803
    8979_38312904del
    GRCh37.p13First PassNC_000019.9Chr1938,038,97938,312,904

    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)
    nssv184235704e-061276146
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