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nsv6613225

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,212

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 84 SVs from 25 studies. See in: genome view    
    Submitted genomic77,604,354-77,605,565Question Mark
    Overlapping variant regions from other studies: 85 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):77,233,671-77,234,882Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6613225Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr777,604,35477,605,565
    nsv6613225RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr777,233,67177,234,882

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18158875deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18158875Submitted genomicNC_000007.14:g.776
    04354_77605565del
    GRCh38 (hg38)NC_000007.14Chr777,604,35477,605,565
    nssv18158875RemappedPerfectNC_000007.13:g.772
    33671_77234882del
    GRCh37.p13First PassNC_000007.13Chr777,233,67177,234,882

    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)
    nssv18158875<0.001138010
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