A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11498n54



Internal ID22779393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90537591..90592034hg38UCSC Ensembl
chr7:90166905..90221348hg19UCSC Ensembl
chr7:90004841..90059284hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3854444
hg1954444
hg1854444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607789, nsv607790
SamplesHGDP01198, HGDP00776
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11498n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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