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nsv6419323

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,190

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 125 SVs from 34 studies. See in: genome view    
    Submitted genomic128,796,758-128,797,947Question Mark
    Overlapping variant regions from other studies: 125 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):128,436,812-128,438,001Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6419323Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7128,796,758128,797,947
    nsv6419323RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7128,436,812128,438,001

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18153326deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18153326Submitted genomicNC_000007.14:g.128
    796758_128797947de
    l
    GRCh38 (hg38)NC_000007.14Chr7128,796,758128,797,947
    nssv18153326RemappedPerfectNC_000007.13:g.128
    436812_128438001de
    l
    GRCh37.p13First PassNC_000007.13Chr7128,436,812128,438,001

    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)
    nssv18153326<0.0011538004
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