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nsv7076758

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:102,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 371 SVs from 61 studies. See in: genome view    
    Submitted genomic30,519,473-30,621,872Question Mark
    Overlapping variant regions from other studies: 371 SVs from 61 studies. See in: genome view    
    Remapped(Score: Perfect):28,846,491-28,948,890Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7076758Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1730,519,47330,621,872
    nsv7076758RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1728,846,49128,948,890

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756950inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756950Submitted genomicNC_000017.11:g.305
    19473_30621872inv
    GRCh38 (hg38)NC_000017.11Chr1730,519,47330,621,872
    nssv18756950RemappedPerfectNC_000017.10:g.288
    46491_28948890inv
    GRCh37.p13First PassNC_000017.10Chr1728,846,49128,948,890

    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)
    nssv187569504e-061276268
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