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nsv6317192

  • 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: 209 SVs from 32 studies. See in: genome view    
    Submitted genomic196,730,101-196,732,200Question Mark
    Overlapping variant regions from other studies: 209 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):196,699,231-196,701,330Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6317192Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1196,730,101196,732,200
    nsv6317192RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1196,699,231196,701,330

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18056602deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18056602Submitted genomicNC_000001.11:g.196
    730101_196732200de
    l
    GRCh38 (hg38)NC_000001.11Chr1196,730,101196,732,200
    nssv18056602RemappedPerfectNC_000001.10:g.196
    699231_196701330de
    l
    GRCh37.p13First PassNC_000001.10Chr1196,699,231196,701,330

    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)
    nssv18056602<0.0011738430
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