A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4463n54



Internal ID18996639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34412954..34414565hg38UCSC Ensembl
chr15:34705155..34706766hg19UCSC Ensembl
chr15:32492447..32494058hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381612
hg191612
hg181612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568946, nsv568948, nsv568947
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4463n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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