A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664858



Internal ID15401510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:41079743..41084624hg38UCSC Ensembl
Innerchr5:41079845..41084726hg19UCSC Ensembl
Innerchr5:41115602..41120483hg18UCSC Ensembl
Innerchr5:41115602..41120483hg17UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg384882
hg194882
hg184882
hg174882
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515813
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664858
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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