A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585194



Internal ID16372603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:874038..894725hg38UCSC Ensembl
Innerchr20:854681..875368hg19UCSC Ensembl
Innerchr20:802681..823368hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3820688
hg1920688
hg1820688
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150945
SamplesNINDS_64
Known GenesANGPT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585194
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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