A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9639n54



Internal ID22777534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:18985993..19271224hg38UCSC Ensembl
chr5:18986102..19271333hg19UCSC Ensembl
chr5:19021859..19307090hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38285232
hg19285232
hg18285232
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597404, nsv597399
SamplesNINDS_91
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9639n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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