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nsv6357210

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:94

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 115 SVs from 27 studies. See in: genome view    
    Submitted genomic73,833,623-73,833,716Question Mark
    Overlapping variant regions from other studies: 115 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):73,882,774-73,882,867Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6357210Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr373,833,62373,833,716
    nsv6357210RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr373,882,77473,882,867

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18102486deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18102486Submitted genomicNC_000003.12:g.738
    33623_73833716del
    GRCh38 (hg38)NC_000003.12Chr373,833,62373,833,716
    nssv18102486RemappedPerfectNC_000003.11:g.738
    82774_73882867del
    GRCh37.p13First PassNC_000003.11Chr373,882,77473,882,867

    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)
    nssv181024860.00417038126
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