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nsv6790494

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,302

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 68 SVs from 20 studies. See in: genome view    
    Submitted genomic175,504,884-175,507,185Question Mark
    Overlapping variant regions from other studies: 68 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):174,931,887-174,934,188Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6790494Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5175,504,884175,507,185
    nsv6790494RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5174,931,887174,934,188

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18508698deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18508698Submitted genomicNC_000005.10:g.175
    504884_175507185de
    l
    GRCh38 (hg38)NC_000005.10Chr5175,504,884175,507,185
    nssv18508698RemappedPerfectNC_000005.9:g.1749
    31887_174934188del
    GRCh37.p13First PassNC_000005.9Chr5174,931,887174,934,188

    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)
    nssv185086981.1e-053275868
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