A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522879



Internal ID15450172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:5308998..5322007hg38UCSC Ensembl
Innerchr20:5289644..5302653hg19UCSC Ensembl
Innerchr20:5237644..5250653hg18UCSC Ensembl
Innerchr20:5237644..5250653hg17UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3813010
hg1913010
hg1813010
hg1713010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698535
Samples
Known GenesPROKR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522879
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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