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nsv7039995

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:674,077

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1665 SVs from 75 studies. See in: genome view    
    Submitted genomic57,602,974-58,277,050Question Mark
    Overlapping variant regions from other studies: 1665 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):57,588,701-58,262,777Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039995Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr357,602,97458,277,050
    nsv7039995RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr357,588,70158,262,777

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18771397inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18771397Submitted genomicNC_000003.12:g.576
    02974_58277050inv
    GRCh38 (hg38)NC_000003.12Chr357,602,97458,277,050
    nssv18771397RemappedPerfectNC_000003.11:g.575
    88701_58262777inv
    GRCh37.p13First PassNC_000003.11Chr357,588,70158,262,777

    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)
    nssv18771397<0.001135271882
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