A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4008814



Internal ID22070445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:60048698..60063082hg38UCSC Ensembl
Outerchr16:60042592..60071814hg38UCSC Ensembl
Innerchr16:60082602..60096986hg19UCSC Ensembl
Outerchr16:60076496..60105718hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3829223
hg1929223
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155328
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4008814
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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