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nsv6326700

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,541

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 108 SVs from 32 studies. See in: genome view    
    Submitted genomic19,979,683-19,986,223Question Mark
    Overlapping variant regions from other studies: 108 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):20,306,176-20,312,716Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6326700Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr119,979,68319,986,223
    nsv6326700RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr120,306,17620,312,716

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18056571deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18056571Submitted genomicNC_000001.11:g.199
    79683_19986223del
    GRCh38 (hg38)NC_000001.11Chr119,979,68319,986,223
    nssv18056571RemappedPerfectNC_000001.10:g.203
    06176_20312716del
    GRCh37.p13First PassNC_000001.10Chr120,306,17620,312,716

    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)
    nssv18056571<0.001139146
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