A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11454n54



Internal ID22779349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75708326..75741050hg38UCSC Ensembl
chr7:75337644..75370368hg19UCSC Ensembl
chr7:75175580..75208304hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3832725
hg1932725
hg1832725
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607512, nsv607514
Samples
Known GenesHIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11454n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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