A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4010477



Internal ID22072108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:2655940..2691811hg38UCSC Ensembl
Outerchr16:2629667..2697856hg38UCSC Ensembl
Innerchr16:2705941..2741812hg19UCSC Ensembl
Outerchr16:2679668..2747857hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3868190
hg1968190
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155220
Supporting Variants
Samples
Known GenesERVK13-1, FLJ42627, KCTD5, LOC652276
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4010477
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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