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nsv7001221

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17,799

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 201 SVs from 36 studies. See in: genome view    
    Submitted genomic36,416,490-36,434,288Question Mark
    Overlapping variant regions from other studies: 201 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):36,907,392-36,925,190Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7001221Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,416,49036,434,288
    nsv7001221RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,907,39236,925,190

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18423264deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18423264Submitted genomicNC_000019.10:g.364
    16490_36434288del
    GRCh38 (hg38)NC_000019.10Chr1936,416,49036,434,288
    nssv18423264RemappedPerfectNC_000019.9:g.3690
    7392_36925190del
    GRCh37.p13First PassNC_000019.9Chr1936,907,39236,925,190

    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)
    nssv184232643.2e-059276184
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