A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11664n54



Internal ID22779559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143848626..144177097hg38UCSC Ensembl
chr7:143545719..143874190hg19UCSC Ensembl
chr7:143176652..143505123hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38328472
hg19328472
hg18328472
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv608694, nsv608693, nsv608692
SamplesHGDP00013, HGDP01293, NINDS_149
Known GenesFAM115A, OR2A12, OR2A14, OR2A2, OR2A25, OR2A5, OR2F1, OR2F2, OR6B1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11664n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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