A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6196n54



Internal ID20139620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1222317..1245701hg38UCSC Ensembl
chr19:1222316..1245700hg19UCSC Ensembl
chr19:1173316..1196700hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3823385
hg1923385
hg1823385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578271, nsv578270, nsv578269
Samples
Known GenesATP5D, C19orf26, STK11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6196n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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