U.S. flag

An official website of the United States government

nsv6351638

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:776

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 338 SVs from 43 studies. See in: genome view    
    Submitted genomic241,590,100-241,590,875Question Mark
    Overlapping variant regions from other studies: 338 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):242,529,515-242,530,290Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6351638Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2241,590,100241,590,875
    nsv6351638RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2242,529,515242,530,290

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18209020duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18209020Submitted genomicNC_000002.12:g.241
    590100_241590875du
    p
    GRCh38 (hg38)NC_000002.12Chr2241,590,100241,590,875
    nssv18209020RemappedPerfectNC_000002.11:g.242
    529515_242530290du
    p
    GRCh37.p13First PassNC_000002.11Chr2242,529,515242,530,290

    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)
    nssv182090200.941982421092
    Support Center