U.S. flag

An official website of the United States government

nsv6985134

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,623

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 234 SVs from 31 studies. See in: genome view    
    Submitted genomic75,618,306-75,620,928Question Mark
    Overlapping variant regions from other studies: 234 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):73,614,386-73,617,008Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6985134Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1775,618,30675,620,928
    nsv6985134RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1773,614,38673,617,008

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18415258deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18415258Submitted genomicNC_000017.11:g.756
    18306_75620928del
    GRCh38 (hg38)NC_000017.11Chr1775,618,30675,620,928
    nssv18415258RemappedPerfectNC_000017.10:g.736
    14386_73617008del
    GRCh37.p13First PassNC_000017.10Chr1773,614,38673,617,008

    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)
    nssv184152584e-061275858
    Support Center