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nsv6934303

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,241

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 137 SVs from 36 studies. See in: genome view    
    Submitted genomic75,339,422-75,348,662Question Mark
    Overlapping variant regions from other studies: 137 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):75,733,202-75,742,442Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6934303Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1275,339,42275,348,662
    nsv6934303RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1275,733,20275,742,442

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18371985deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18371985Submitted genomicNC_000012.12:g.753
    39422_75348662del
    GRCh38 (hg38)NC_000012.12Chr1275,339,42275,348,662
    nssv18371985RemappedPerfectNC_000012.11:g.757
    33202_75742442del
    GRCh37.p13First PassNC_000012.11Chr1275,733,20275,742,442

    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)
    nssv183719857e-062275936
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