A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4408n54



Internal ID20137832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27158056..27164655hg38UCSC Ensembl
chr15:27403203..27409802hg19UCSC Ensembl
chr15:24985949..24992548hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg386600
hg196600
hg186600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568656, nsv568657, nsv568658
Samples
Known GenesGABRG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4408n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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