A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5322n54



Internal ID18997498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89390106..89421804hg38UCSC Ensembl
chr16:89456514..89488212hg19UCSC Ensembl
chr16:87984015..88015713hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3831699
hg1931699
hg1831699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573736, nsv573737
Samples
Known GenesANKRD11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5322n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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