A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9634n54



Internal ID22777529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:18665041..18726907hg38UCSC Ensembl
chr5:18665150..18727016hg19UCSC Ensembl
chr5:18700907..18762773hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3861867
hg1961867
hg1861867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597377, nsv597375
Samples1782681169_A, 1780854566_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9634n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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