A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv191n54



Internal ID20133615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23874282..23874867hg38UCSC Ensembl
chr1:24200772..24201357hg19UCSC Ensembl
chr1:24073359..24073944hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38586
hg19586
hg18586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv545779, nsv545780
Samples
Known GenesCNR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv191n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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