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nsv6447100

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:112,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 368 SVs from 54 studies. See in: genome view    
    Submitted genomic122,832,501-122,945,100Question Mark
    Overlapping variant regions from other studies: 368 SVs from 54 studies. See in: genome view    
    Remapped(Score: Perfect):125,594,780-125,707,379Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6447100Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9122,832,501122,945,100
    nsv6447100RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9125,594,780125,707,379

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18234929duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18234929Submitted genomicNC_000009.12:g.122
    832501_122945100du
    p
    GRCh38 (hg38)NC_000009.12Chr9122,832,501122,945,100
    nssv18234929RemappedPerfectNC_000009.11:g.125
    594780_125707379du
    p
    GRCh37.p13First PassNC_000009.11Chr9125,594,780125,707,379

    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)
    nssv18234929<0.0011539214
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