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nsv6789557

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 151 SVs from 40 studies. See in: genome view    
    Submitted genomic128,977,301-128,989,900Question Mark
    Overlapping variant regions from other studies: 151 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):128,312,994-128,325,593Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6789557Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5128,977,301128,989,900
    nsv6789557RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5128,312,994128,325,593

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18506522deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18506522Submitted genomicNC_000005.10:g.128
    977301_128989900de
    l
    GRCh38 (hg38)NC_000005.10Chr5128,977,301128,989,900
    nssv18506522RemappedPerfectNC_000005.9:g.1283
    12994_128325593del
    GRCh37.p13First PassNC_000005.9Chr5128,312,994128,325,593

    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)
    nssv185065224e-060276012
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