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nsv7052009

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,869

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 936 SVs from 76 studies. See in: genome view    
    Submitted genomic241,968,070-241,976,938Question Mark
    Overlapping variant regions from other studies: 936 SVs from 76 studies. See in: genome view    
    Remapped(Score: Perfect):242,910,221-242,919,089Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052009Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2241,968,070241,976,938
    nsv7052009RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2242,910,221242,919,089

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18769106inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18769106Submitted genomicNC_000002.12:g.241
    968070_241976938in
    v
    GRCh38 (hg38)NC_000002.12Chr2241,968,070241,976,938
    nssv18769106RemappedPerfectNC_000002.11:g.242
    910221_242919089in
    v
    GRCh37.p13First PassNC_000002.11Chr2242,910,221242,919,089

    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)
    nssv187691062.5e-057275000
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