A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6591n54



Internal ID20140015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56407229..56561064hg38UCSC Ensembl
chr19:56918598..57072433hg19UCSC Ensembl
chr19:61610410..61764245hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38153836
hg19153836
hg18153836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv580385, nsv580386
Samples
Known GenesZFP28, ZNF471, ZNF583, ZNF667, ZNF667-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6591n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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