A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585725



Internal ID16373134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23663750..23795182hg38UCSC Ensembl
Innerchr20:23644387..23775819hg19UCSC Ensembl
Innerchr20:23592387..23723819hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38131433
hg19131433
hg18131433
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152374
SamplesNINDS_265
Known GenesCST1, CST4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585725
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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