A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2841n54



Internal ID20136265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104137402..104138381hg38UCSC Ensembl
chr12:104531180..104532159hg19UCSC Ensembl
chr12:103055310..103056289hg18UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38980
hg19980
hg18980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv560049, nsv560050
Samples
Known GenesNFYB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2841n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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