A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155220



Internal ID22085725
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010476, nssv4010477
Samples
Known GenesERVK13-1, FLJ42627, KCTD5, LOC652276
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155220
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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