A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12997n54



Internal ID22780892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135906649..135908222hg38UCSC Ensembl
chr9:138798495..138800068hg19UCSC Ensembl
chr9:137938316..137939889hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381574
hg191574
hg181574
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615938, nsv615933, nsv615939, nsv615934
Samples
Known GenesCAMSAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12997n54
Frequency
Sample Size17421
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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