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nsv6707160

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,815

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 76 SVs from 22 studies. See in: genome view    
    Submitted genomic37,284,953-37,288,767Question Mark
    Overlapping variant regions from other studies: 76 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):37,326,444-37,330,258Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6707160Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr337,284,95337,288,767
    nsv6707160RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr337,326,44437,330,258

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18483522deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18483522Submitted genomicNC_000003.12:g.372
    84953_37288767del
    GRCh38 (hg38)NC_000003.12Chr337,284,95337,288,767
    nssv18483522RemappedPerfectNC_000003.11:g.373
    26444_37330258del
    GRCh37.p13First PassNC_000003.11Chr337,326,44437,330,258

    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)
    nssv184835224e-061275714
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