A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11483n54



Internal ID22779378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80007366..80063734hg38UCSC Ensembl
chr7:79636682..79693050hg19UCSC Ensembl
chr7:79474618..79530986hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3856369
hg1956369
hg1856369
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607677, nsv607676
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11483n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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