A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1017984



Internal ID16311940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185519679..185522869hg38UCSC Ensembl
Innerchr4:186440833..186444023hg19UCSC Ensembl
Innerchr4:186677827..186681017hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg383191
hg193191
hg183191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596375
Supporting Variants
Samples
Known GenesPDLIM3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1017984
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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