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nsv6330865

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:458

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 100 SVs from 21 studies. See in: genome view    
    Submitted genomic151,845,401-151,845,858Question Mark
    Overlapping variant regions from other studies: 111 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):151,817,877-151,818,334Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6330865Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1151,845,401151,845,858
    nsv6330865RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1151,817,877151,818,334

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18051351deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18051351Submitted genomicNC_000001.11:g.151
    845401_151845858de
    l
    GRCh38 (hg38)NC_000001.11Chr1151,845,401151,845,858
    nssv18051351RemappedPerfectNC_000001.10:g.151
    817877_151818334de
    l
    GRCh37.p13First PassNC_000001.10Chr1151,817,877151,818,334

    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)
    nssv18051351<0.001134626
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