A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2941n54



Internal ID20136365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124540407..124541609hg38UCSC Ensembl
chr12:125024953..125026155hg19UCSC Ensembl
chr12:123590906..123592108hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381203
hg191203
hg181203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv560568, nsv560560, nsv560569
Samples
Known GenesNCOR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2941n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer