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nsv7030230

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:257

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 115 SVs from 24 studies. See in: genome view    
    Submitted genomic32,700,954-32,701,210Question Mark
    Overlapping variant regions from other studies: 115 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):31,288,756-31,289,012Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7030230Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2032,700,95432,701,210
    nsv7030230RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2031,288,75631,289,012

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18431241deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18431241Submitted genomicNC_000020.11:g.327
    00954_32701210del
    GRCh38 (hg38)NC_000020.11Chr2032,700,95432,701,210
    nssv18431241RemappedPerfectNC_000020.10:g.312
    88756_31289012del
    GRCh37.p13First PassNC_000020.10Chr2031,288,75631,289,012

    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)
    nssv184312410.003705252906
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