A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2774n54



Internal ID20136198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:89708471..89709574hg38UCSC Ensembl
chr12:90102248..90103351hg19UCSC Ensembl
chr12:88626379..88627482hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg381104
hg191104
hg181104
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv559716, nsv559707, nsv559714
Samples
Known GenesLINC00936
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2774n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss4
Observed Complex0
Frequencyn/a


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