A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6291n54



Internal ID22774186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15928643..15931253hg38UCSC Ensembl
chr19:16039453..16042063hg19UCSC Ensembl
chr19:15900453..15903063hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382611
hg192611
hg182611
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578733, nsv578732
Samples
Known GenesCYP4F11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6291n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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