A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4917n54



Internal ID18997093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14693830..14704088hg38UCSC Ensembl
chr16:14787687..14797945hg19UCSC Ensembl
chr16:14695188..14705446hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3810259
hg1910259
hg1810259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571510, nsv571512
Samples
Known GenesPLA2G10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4917n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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