A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5173n54



Internal ID22773068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62680059..62766677hg38UCSC Ensembl
chr16:62713963..62800581hg19UCSC Ensembl
chr16:61271464..61358082hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3886619
hg1986619
hg1886619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv572873, nsv572874
SamplesHGDP00155
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5173n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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