U.S. flag

An official website of the United States government

nsv7066881

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:23,558

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 172 SVs from 38 studies. See in: genome view    
    Submitted genomic87,893,282-87,916,839Question Mark
    Overlapping variant regions from other studies: 172 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):87,604,174-87,627,731Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066881Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1187,893,28287,916,839
    nsv7066881RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1187,604,17487,627,731

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18742845inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18742845Submitted genomicNC_000011.10:g.878
    93282_87916839inv
    GRCh38 (hg38)NC_000011.10Chr1187,893,28287,916,839
    nssv18742845RemappedPerfectNC_000011.9:g.8760
    4174_87627731inv
    GRCh37.p13First PassNC_000011.9Chr1187,604,17487,627,731

    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)
    nssv187428454e-061276268
    Support Center