U.S. flag

An official website of the United States government

nsv7058955

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:320,005

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 651 SVs from 63 studies. See in: genome view    
    Submitted genomic91,431,297-91,751,301Question Mark
    Overlapping variant regions from other studies: 651 SVs from 63 studies. See in: genome view    
    Remapped(Score: Perfect):93,191,054-93,511,058Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058955Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1091,431,29791,751,301
    nsv7058955RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1093,191,05493,511,058

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18738535inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18738535Submitted genomicNC_000010.11:g.914
    31297_91751301inv
    GRCh38 (hg38)NC_000010.11Chr1091,431,29791,751,301
    nssv18738535RemappedPerfectNC_000010.10:g.931
    91054_93511058inv
    GRCh37.p13First PassNC_000010.10Chr1093,191,05493,511,058

    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)
    nssv187385350.0061734269750
    Support Center