A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11499n54



Internal ID22779394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90556437..90599724hg38UCSC Ensembl
chr7:90185751..90229038hg19UCSC Ensembl
chr7:90023687..90066974hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3843288
hg1943288
hg1843288
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607791, nsv607792
SamplesHGDP00715, HGDP00711
Known GenesCDK14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11499n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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