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nsv6646430

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,504

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 116 SVs from 31 studies. See in: genome view    
    Submitted genomic19,605,812-19,612,315Question Mark
    Overlapping variant regions from other studies: 116 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):19,932,306-19,938,809Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6646430Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr119,605,81219,612,315
    nsv6646430RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr119,932,30619,938,809

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18365942deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18365942Submitted genomicNC_000001.11:g.196
    05812_19612315del
    GRCh38 (hg38)NC_000001.11Chr119,605,81219,612,315
    nssv18365942RemappedPerfectNC_000001.10:g.199
    32306_19938809del
    GRCh37.p13First PassNC_000001.10Chr119,932,30619,938,809

    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)
    nssv183659427e-062275144
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