A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4008819



Internal ID22070450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69990686..70179141hg38UCSC Ensembl
Outerchr16:69954483..70200633hg38UCSC Ensembl
Innerchr16:70024589..70213044hg19UCSC Ensembl
Outerchr16:69988386..70234536hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38246151
hg19246151
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155330
Supporting Variants
Samples
Known GenesCLEC18A, CLEC18C, MIR1972-1, MIR1972-2, PDPR, PDXDC2P
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4008819
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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