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nsv7052867

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:76,372

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 257 SVs from 36 studies. See in: genome view    
    Submitted genomic144,287,154-144,363,525Question Mark
    Overlapping variant regions from other studies: 257 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):145,044,721-145,121,092Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052867Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2144,287,154144,363,525
    nsv7052867RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2145,044,721145,121,092

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765892inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765892Submitted genomicNC_000002.12:g.144
    287154_144363525in
    v
    GRCh38 (hg38)NC_000002.12Chr2144,287,154144,363,525
    nssv18765892RemappedPerfectNC_000002.11:g.145
    044721_145121092in
    v
    GRCh37.p13First PassNC_000002.11Chr2145,044,721145,121,092

    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)
    nssv187658924e-060276266
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