A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852782



Internal ID15800052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14694625..14704088hg38UCSC Ensembl
Innerchr16:14788482..14797945hg19UCSC Ensembl
Innerchr16:14695983..14705446hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg389464
hg199464
hg189464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571512
Supporting Variants
Samples
Known GenesPLA2G10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852782
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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