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nsv7064020

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,144,157

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8530 SVs from 110 studies. See in: genome view    
    Submitted genomic48,004,601-50,148,757Question Mark
    Overlapping variant regions from other studies: 8530 SVs from 110 studies. See in: genome view    
    Remapped(Score: Perfect):48,507,858-50,652,014Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7064020Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1948,004,60150,148,757
    nsv7064020RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1948,507,85850,652,014

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760833inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760833Submitted genomicNC_000019.10:g.480
    04601_50148757inv
    GRCh38 (hg38)NC_000019.10Chr1948,004,60150,148,757
    nssv18760833RemappedPerfectNC_000019.9:g.4850
    7858_50652014inv
    GRCh37.p13First PassNC_000019.9Chr1948,507,85850,652,014

    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)
    nssv187608334e-061276268
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