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nsv6370850

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 100 SVs from 24 studies. See in: genome view    
    Submitted genomic49,411,301-49,412,000Question Mark
    Overlapping variant regions from other studies: 100 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):49,448,734-49,449,433Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6370850Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr349,411,30149,412,000
    nsv6370850RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr349,448,73449,449,433

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18102663deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18102663Submitted genomicNC_000003.12:g.494
    11301_49412000del
    GRCh38 (hg38)NC_000003.12Chr349,411,30149,412,000
    nssv18102663RemappedPerfectNC_000003.11:g.494
    48734_49449433del
    GRCh37.p13First PassNC_000003.11Chr349,448,73449,449,433

    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)
    nssv181026630.043164137852
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