A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11283n54



Internal ID22779178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39503235..39512120hg38UCSC Ensembl
chr7:39542834..39551719hg19UCSC Ensembl
chr7:39509359..39518244hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg388886
hg198886
hg188886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv606680, nsv606676, nsv606675, nsv606679
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11283n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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