A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12689n54



Internal ID22780584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39409405..39444669hg38UCSC Ensembl
chr9:39409402..39444668hg19UCSC Ensembl
chr9:39399402..39434668hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3835265
hg1935267
hg1835267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614285, nsv614286
Samples
Known GenesLOC653501, ZNF658B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12689n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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