A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4884n54



Internal ID22772779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4315622..4317103hg38UCSC Ensembl
chr16:4365623..4367104hg19UCSC Ensembl
chr16:4305624..4307105hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381482
hg191482
hg181482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571297, nsv571299, nsv571296
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4884n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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