A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4464n54



Internal ID20137888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34412954..34414928hg38UCSC Ensembl
chr15:34705155..34707129hg19UCSC Ensembl
chr15:32492447..32494421hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381975
hg191975
hg181975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568949, nsv568962
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4464n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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