A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652669



Internal ID15042635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:53152684..53194326hg38UCSC Ensembl
Innerchr3:53186700..53228342hg19UCSC Ensembl
Innerchr3:53161740..53203382hg18UCSC Ensembl
Innerchr3:53161740..53203382hg17UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3841643
hg1941643
hg1841643
hg1741643
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517233
Supporting Variants
Samples
Known GenesPRKCD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv652669
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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