A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4965n54



Internal ID22772860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28390583..28407135hg38UCSC Ensembl
chr16:28401904..28418456hg19UCSC Ensembl
chr16:28309405..28325957hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3816553
hg1916553
hg1816553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571725, nsv571726
Samples
Known GenesEIF3C, EIF3CL, MIR6862-1, MIR6862-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4965n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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