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nsv7017521

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 100 SVs from 27 studies. See in: genome view    
    Submitted genomic17,527,101-17,529,200Question Mark
    Overlapping variant regions from other studies: 100 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):17,637,910-17,640,009Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7017521Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1917,527,10117,529,200
    nsv7017521RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1917,637,91017,640,009

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18421450deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18421450Submitted genomicNC_000019.10:g.175
    27101_17529200del
    GRCh38 (hg38)NC_000019.10Chr1917,527,10117,529,200
    nssv18421450RemappedPerfectNC_000019.9:g.1763
    7910_17640009del
    GRCh37.p13First PassNC_000019.9Chr1917,637,91017,640,009

    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)
    nssv18421450<0.00169253632
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