A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155323



Internal ID22085828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55762477..55795678hg38UCSC Ensembl
Outerchr16:55761302..55808442hg38UCSC Ensembl
Innerchr16:55796389..55829590hg19UCSC Ensembl
Outerchr16:55795214..55842354hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3847141
hg1947141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv118n97
Supporting Variantsnssv4008744
Samples
Known GenesCES1, CES1P1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155323
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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