A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151201



Internal ID15530138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:9433786..9457525hg38UCSC Ensembl
Innerchr20:9414433..9438172hg19UCSC Ensembl
Innerchr20:9362433..9386172hg18UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3823740
hg1923740
hg1823740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585410
Supporting Variants
SamplesHGDP00900
Known GenesPLCB4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151201
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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