A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11453n54



Internal ID22779348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75700353..75752244hg38UCSC Ensembl
chr7:75329671..75381562hg19UCSC Ensembl
chr7:75167607..75219498hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3851892
hg1951892
hg1851892
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607511, nsv607513
SamplesNINDS_147
Known GenesHIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11453n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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