A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4482n54



Internal ID18996658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34462473..34546808hg38UCSC Ensembl
chr15:34754674..34839009hg19UCSC Ensembl
chr15:32541966..32626301hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3884336
hg1984336
hg1884336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569119, nsv569116, nsv569117
Samples
Known GenesGOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4482n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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