A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6320n54



Internal ID20139744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21403995..21426805hg38UCSC Ensembl
chr19:21586797..21609607hg19UCSC Ensembl
chr19:21378637..21401447hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3822811
hg1922811
hg1822811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578954, nsv578953
Samples
Known GenesZNF493
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6320n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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