A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2295n54



Internal ID20135719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3199100..3200891hg38UCSC Ensembl
chr12:3308266..3310057hg19UCSC Ensembl
chr12:3178527..3180318hg18UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg381792
hg191792
hg181792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv557108, nsv557109
Samples
Known GenesTSPAN9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2295n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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