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nsv7049962

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,830,890

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 6890 SVs from 99 studies. See in: genome view    
    Submitted genomic227,539,172-230,370,061Question Mark
    Overlapping variant regions from other studies: 6890 SVs from 99 studies. See in: genome view    
    Remapped(Score: Perfect):228,403,888-231,234,776Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7049962Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2227,539,172230,370,061
    nsv7049962RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2228,403,888231,234,776

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18768120inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18768120Submitted genomicNC_000002.12:g.227
    539172_230370061in
    v
    GRCh38 (hg38)NC_000002.12Chr2227,539,172230,370,061
    nssv18768120RemappedPerfectNC_000002.11:g.228
    403888_231234776in
    v
    GRCh37.p13First PassNC_000002.11Chr2228,403,888231,234,776

    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)
    nssv187681200.0174564271504
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