A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11026n54



Internal ID20144450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163413723..163415657hg38UCSC Ensembl
chr6:163834755..163836689hg19UCSC Ensembl
chr6:163754745..163756679hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381935
hg191935
hg181935
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605203, nsv605206, nsv605198, nsv605202, nsv605199
Samples
Known GenesCAHM, QKI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11026n54
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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