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nsv6730424

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:45

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 97 SVs from 20 studies. See in: genome view    
    Submitted genomic172,043,001-172,043,045Question Mark
    Overlapping variant regions from other studies: 97 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):171,760,791-171,760,835Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6730424Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3172,043,001172,043,045
    nsv6730424RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3171,760,791171,760,835

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18476816deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18476816Submitted genomicNC_000003.12:g.172
    043001_172043045de
    l
    GRCh38 (hg38)NC_000003.12Chr3172,043,001172,043,045
    nssv18476816RemappedPerfectNC_000003.11:g.171
    760791_171760835de
    l
    GRCh37.p13First PassNC_000003.11Chr3171,760,791171,760,835

    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)
    nssv18476816<0.00190232170
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