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nsv6415030

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,738

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 94 SVs from 31 studies. See in: genome view    
    Submitted genomic157,421,247-157,425,984Question Mark
    Overlapping variant regions from other studies: 94 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):156,848,255-156,852,992Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6415030Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5157,421,247157,425,984
    nsv6415030RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5156,848,255156,852,992

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18127743deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18127743Submitted genomicNC_000005.10:g.157
    421247_157425984de
    l
    GRCh38 (hg38)NC_000005.10Chr5157,421,247157,425,984
    nssv18127743RemappedPerfectNC_000005.9:g.1568
    48255_156852992del
    GRCh37.p13First PassNC_000005.9Chr5156,848,255156,852,992

    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)
    nssv18127743<0.001239048
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