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nsv6602402

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:127,858

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 573 SVs from 66 studies. See in: genome view    
    Submitted genomic66,947,709-67,075,566Question Mark
    Overlapping variant regions from other studies: 572 SVs from 66 studies. See in: genome view    
    Remapped(Score: Perfect):66,412,696-66,540,553Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6602402Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr766,947,70967,075,566
    nsv6602402RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr766,412,69666,540,553

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18236118duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18236118Submitted genomicNC_000007.14:g.669
    47709_67075566dup
    GRCh38 (hg38)NC_000007.14Chr766,947,70967,075,566
    nssv18236118RemappedPerfectNC_000007.13:g.664
    12696_66540553dup
    GRCh37.p13First PassNC_000007.13Chr766,412,69666,540,553

    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)
    nssv18236118<0.001139292
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