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nsv7039078

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:108,207

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 581 SVs from 66 studies. See in: genome view    
    Submitted genomic169,426,957-169,535,163Question Mark
    Overlapping variant regions from other studies: 581 SVs from 66 studies. See in: genome view    
    Remapped(Score: Perfect):170,283,467-170,391,673Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039078Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2169,426,957169,535,163
    nsv7039078RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2170,283,467170,391,673

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18768635inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18768635Submitted genomicNC_000002.12:g.169
    426957_169535163in
    v
    GRCh38 (hg38)NC_000002.12Chr2169,426,957169,535,163
    nssv18768635RemappedPerfectNC_000002.11:g.170
    283467_170391673in
    v
    GRCh37.p13First PassNC_000002.11Chr2170,283,467170,391,673

    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)
    nssv187686354e-061276268
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