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nsv6503997

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,251

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 129 SVs from 34 studies. See in: genome view    
    Submitted genomic95,660,084-95,678,334Question Mark
    Overlapping variant regions from other studies: 129 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):96,126,421-96,144,671Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6503997Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1495,660,08495,678,334
    nsv6503997RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1496,126,42196,144,671

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18022214deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18022214Submitted genomicNC_000014.9:g.9566
    0084_95678334del
    GRCh38 (hg38)NC_000014.9Chr1495,660,08495,678,334
    nssv18022214RemappedPerfectNC_000014.8:g.9612
    6421_96144671del
    GRCh37.p13First PassNC_000014.8Chr1496,126,42196,144,671

    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)
    nssv18022214<0.001639254
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