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nsv7015671

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,948

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 84 SVs from 20 studies. See in: genome view    
    Submitted genomic9,290,735-9,304,682Question Mark
    Overlapping variant regions from other studies: 84 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):9,401,411-9,415,358Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7015671Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr199,290,7359,304,682
    nsv7015671RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr199,401,4119,415,358

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18637424duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18637424Submitted genomicNC_000019.10:g.929
    0735_9304682dup
    GRCh38 (hg38)NC_000019.10Chr199,290,7359,304,682
    nssv18637424RemappedPerfectNC_000019.9:g.9401
    411_9415358dup
    GRCh37.p13First PassNC_000019.9Chr199,401,4119,415,358

    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)
    nssv186374244e-061275790
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