A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12671n54



Internal ID22780566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36487146..36488264hg38UCSC Ensembl
chr9:36487143..36488261hg19UCSC Ensembl
chr9:36477143..36478261hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg381119
hg191119
hg181119
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614205, nsv614201
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12671n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss2
Observed Complex0
Frequencyn/a


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