A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10338n54



Internal ID20143762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28954942..29380520hg38UCSC Ensembl
chr6:28922719..29348297hg19UCSC Ensembl
chr6:29030698..29456276hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38425579
hg19425579
hg18425579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601215, nsv601214, nsv601213
Samples
Known GenesLOC100129636, OR12D3, OR14J1, OR2B3, OR2J2, OR2J3, OR2W1, OR5V1, ZNF311
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10338n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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