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nsv6327696

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 134 SVs from 19 studies. See in: genome view    
    Submitted genomic183,535,401-183,538,200Question Mark
    Overlapping variant regions from other studies: 136 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):183,504,536-183,507,335Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6327696Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1183,535,401183,538,200
    nsv6327696RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1183,504,536183,507,335

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18054712deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18054712Submitted genomicNC_000001.11:g.183
    535401_183538200de
    l
    GRCh38 (hg38)NC_000001.11Chr1183,535,401183,538,200
    nssv18054712RemappedPerfectNC_000001.10:g.183
    504536_183507335de
    l
    GRCh37.p13First PassNC_000001.10Chr1183,504,536183,507,335

    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)
    nssv18054712<0.001839024
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