A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8958n54



Internal ID19001134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9366693..9487015hg38UCSC Ensembl
chr4:9368419..9488662hg19UCSC Ensembl
chr4:8977517..9097760hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38120323
hg19120244
hg18120244
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593650, nsv593647, nsv593659
Samples
Known GenesDEFB131, LOC650293, USP17L6P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8958n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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