A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11488n54



Internal ID22779383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84511761..84694195hg38UCSC Ensembl
chr7:84141077..84323511hg19UCSC Ensembl
chr7:83979013..84161447hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38182435
hg19182435
hg18182435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607712, nsv607711, nsv607713
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11488n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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