A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11496n54



Internal ID22779391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:89909309..90080467hg38UCSC Ensembl
chr7:89538623..89709781hg19UCSC Ensembl
chr7:89376559..89547717hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38171159
hg19171159
hg18171159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607773, nsv607772, nsv607774, nsv607775
Samples1780854206_A, NINDS_193, NINDS_149
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11496n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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