A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4008744



Internal ID22070375
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155323
Supporting Variants
Samples
Known GenesCES1, CES1P1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4008744
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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