U.S. flag

An official website of the United States government

nsv7060644

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,969,235

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5475 SVs from 106 studies. See in: genome view    
    Submitted genomic20,030,249-21,999,483Question Mark
    Overlapping variant regions from other studies: 5475 SVs from 106 studies. See in: genome view    
    Remapped(Score: Perfect):20,183,183-22,152,417Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7060644Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1220,030,24921,999,483
    nsv7060644RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1220,183,18322,152,417

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18751131inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18751131Submitted genomicNC_000012.12:g.200
    30249_21999483inv
    GRCh38 (hg38)NC_000012.12Chr1220,030,24921,999,483
    nssv18751131RemappedPerfectNC_000012.11:g.201
    83183_22152417inv
    GRCh37.p13First PassNC_000012.11Chr1220,183,18322,152,417

    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)
    nssv187511314e-061276242
    Support Center