A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6266n54



Internal ID20139690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10102229..10103354hg38UCSC Ensembl
chr19:10212905..10214030hg19UCSC Ensembl
chr19:10073905..10075030hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381126
hg191126
hg181126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578608, nsv578607, nsv578611, nsv578609
Samples
Known GenesANGPTL6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6266n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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