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nsv6818846

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,978

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 124 SVs from 33 studies. See in: genome view    
    Submitted genomic100,066,392-100,069,369Question Mark
    Overlapping variant regions from other studies: 124 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):99,664,015-99,666,992Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6818846Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7100,066,392100,069,369
    nsv6818846RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr799,664,01599,666,992

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18531454deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18531454Submitted genomicNC_000007.14:g.100
    066392_100069369de
    l
    GRCh38 (hg38)NC_000007.14Chr7100,066,392100,069,369
    nssv18531454RemappedPerfectNC_000007.13:g.996
    64015_99666992del
    GRCh37.p13First PassNC_000007.13Chr799,664,01599,666,992

    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)
    nssv185314547e-061276098
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