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nsv6833303

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,134

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 124 SVs from 30 studies. See in: genome view    
    Submitted genomic99,563,414-99,570,547Question Mark
    Overlapping variant regions from other studies: 124 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):99,161,037-99,168,170Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6833303Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr799,563,41499,570,547
    nsv6833303RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr799,161,03799,168,170

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18548337deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18548337Submitted genomicNC_000007.14:g.995
    63414_99570547del
    GRCh38 (hg38)NC_000007.14Chr799,563,41499,570,547
    nssv18548337RemappedPerfectNC_000007.13:g.991
    61037_99168170del
    GRCh37.p13First PassNC_000007.13Chr799,161,03799,168,170

    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)
    nssv185483371.1e-053275926
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