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nsv7017013

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:42,103

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 241 SVs from 35 studies. See in: genome view    
    Submitted genomic36,370,446-36,412,548Question Mark
    Overlapping variant regions from other studies: 241 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):36,861,348-36,903,450Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7017013Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,370,44636,412,548
    nsv7017013RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,861,34836,903,450

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18423259deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18423259Submitted genomicNC_000019.10:g.363
    70446_36412548del
    GRCh38 (hg38)NC_000019.10Chr1936,370,44636,412,548
    nssv18423259RemappedPerfectNC_000019.9:g.3686
    1348_36903450del
    GRCh37.p13First PassNC_000019.9Chr1936,861,34836,903,450

    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)
    nssv184232594e-061276226
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