U.S. flag

An official website of the United States government

nsv7052650

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,810,815

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 13759 SVs from 115 studies. See in: genome view    
    Submitted genomic47,584,744-54,395,558Question Mark
    Overlapping variant regions from other studies: 13761 SVs from 115 studies. See in: genome view    
    Remapped(Score: Perfect):48,050,416-54,861,231Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052650Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr147,584,74454,395,558
    nsv7052650RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr148,050,41654,861,231

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761061inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761061Submitted genomicNC_000001.11:g.475
    84744_54395558inv
    GRCh38 (hg38)NC_000001.11Chr147,584,74454,395,558
    nssv18761061RemappedPerfectNC_000001.10:g.480
    50416_54861231inv
    GRCh37.p13First PassNC_000001.10Chr148,050,41654,861,231

    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)
    nssv187610614e-061276268
    Support Center