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nsv7000001

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:394

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 118 SVs from 23 studies. See in: genome view    
    Submitted genomic2,866,916-2,867,309Question Mark
    Overlapping variant regions from other studies: 118 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):2,866,914-2,867,307Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7000001Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr192,866,9162,867,309
    nsv7000001RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr192,866,9142,867,307

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18636305duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18636305Submitted genomicNC_000019.10:g.286
    6916_2867309dup
    GRCh38 (hg38)NC_000019.10Chr192,866,9162,867,309
    nssv18636305RemappedPerfectNC_000019.9:g.2866
    914_2867307dup
    GRCh37.p13First PassNC_000019.9Chr192,866,9142,867,307

    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)
    nssv186363054e-061225210
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