A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6303n54



Internal ID22774198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19973872..20588017hg38UCSC Ensembl
chr19:20084681..20770823hg19UCSC Ensembl
chr19:19945681..20562663hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38614146
hg19686143
hg18616983
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578802, nsv578801
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF486, ZNF682, ZNF737, ZNF826P, ZNF90
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6303n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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