A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6076n54



Internal ID22773971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76476812..76521109hg38UCSC Ensembl
chr18:74188768..74233066hg19UCSC Ensembl
chr18:72317756..72362054hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3844298
hg1944299
hg1844299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv577687, nsv577686
SamplesNINDS_273
Known GenesFLJ44313, ZNF516
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6076n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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