U.S. flag

An official website of the United States government

nsv7025128

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,826

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 146 SVs from 35 studies. See in: genome view    
    Submitted genomic26,627,299-26,642,124Question Mark
    Overlapping variant regions from other studies: 146 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):27,023,263-27,038,088Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7025128Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2226,627,29926,642,124
    nsv7025128RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2227,023,26327,038,088

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18436701deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18436701Submitted genomicNC_000022.11:g.266
    27299_26642124del
    GRCh38 (hg38)NC_000022.11Chr2226,627,29926,642,124
    nssv18436701RemappedPerfectNC_000022.10:g.270
    23263_27038088del
    GRCh37.p13First PassNC_000022.10Chr2227,023,26327,038,088

    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)
    nssv184367014e-061276224
    Support Center