U.S. flag

An official website of the United States government

nsv6918657

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:142,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 639 SVs from 65 studies. See in: genome view    
    Submitted genomic30,367,401-30,509,500Question Mark
    Overlapping variant regions from other studies: 639 SVs from 65 studies. See in: genome view    
    Remapped(Score: Perfect):30,941,538-31,083,637Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6918657Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1330,367,40130,509,500
    nsv6918657RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1330,941,53831,083,637

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18600873duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18600873Submitted genomicNC_000013.11:g.303
    67401_30509500dup
    GRCh38 (hg38)NC_000013.11Chr1330,367,40130,509,500
    nssv18600873RemappedPerfectNC_000013.10:g.309
    41538_31083637dup
    GRCh37.p13First PassNC_000013.10Chr1330,941,53831,083,637

    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)
    nssv18600873<0.00135260776
    Support Center