A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9166n54



Internal ID22777061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:91457930..91977158hg38UCSC Ensembl
chr4:92379081..92898309hg19UCSC Ensembl
chr4:92598104..93117332hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38519229
hg19519229
hg18519229
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv594863, nsv594861
Samples
Known GenesCCSER1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9166n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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