A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6071n54



Internal ID22773966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76392971..76394780hg38UCSC Ensembl
chr18:74104927..74106736hg19UCSC Ensembl
chr18:72233915..72235724hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381810
hg191810
hg181810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv577676, nsv577674, nsv577668, nsv577669
Samples
Known GenesZNF516
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6071n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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