A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11487n54



Internal ID22779382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:83866564..83904638hg38UCSC Ensembl
chr7:83495880..83533954hg19UCSC Ensembl
chr7:83333816..83371890hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3838075
hg1938075
hg1838075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607709, nsv607708
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11487n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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