A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659928



Internal ID15049894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15719660..15720369hg38UCSC Ensembl
Innerchr5:15719769..15720478hg19UCSC Ensembl
Innerchr5:15772769..15773478hg18UCSC Ensembl
Innerchr5:15772769..15773478hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38710
hg19710
hg18710
hg17710
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516929
Supporting Variants
Samples
Known GenesFBXL7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659928
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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