A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11484n54



Internal ID22779379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81236837..81318201hg38UCSC Ensembl
chr7:80866153..80947517hg19UCSC Ensembl
chr7:80704089..80785453hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3881365
hg1981365
hg1881365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607688, nsv607687
Samples1780854261_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11484n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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