A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv190n54



Internal ID20133614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23874034..23874672hg38UCSC Ensembl
chr1:24200524..24201162hg19UCSC Ensembl
chr1:24073111..24073749hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38639
hg19639
hg18639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv545775, nsv545777, nsv545776
Samples
Known GenesCNR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv190n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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