A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12669n54



Internal ID22780564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36487146..36488025hg38UCSC Ensembl
chr9:36487143..36488022hg19UCSC Ensembl
chr9:36477143..36478022hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38880
hg19880
hg18880
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614206, nsv614198, nsv614209
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12669n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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