A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593727



Internal ID16034450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10395703..10693367hg38UCSC Ensembl
Innerchr4:10397327..10694991hg19UCSC Ensembl
Innerchr4:10006425..10304089hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38297665
hg19297665
hg18297665
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv993049
Samples
Known GenesCLNK, ZNF518B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593727
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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