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nsv6925618

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 125 SVs from 30 studies. See in: genome view    
    Submitted genomic75,338,201-75,342,900Question Mark
    Overlapping variant regions from other studies: 125 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):75,731,981-75,736,680Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6925618Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1275,338,20175,342,900
    nsv6925618RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1275,731,98175,736,680

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18371984deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18371984Submitted genomicNC_000012.12:g.753
    38201_75342900del
    GRCh38 (hg38)NC_000012.12Chr1275,338,20175,342,900
    nssv18371984RemappedPerfectNC_000012.11:g.757
    31981_75736680del
    GRCh37.p13First PassNC_000012.11Chr1275,731,98175,736,680

    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)
    nssv183719842.1e-056275666
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