A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155226



Internal ID22085731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8443816..8558535hg38UCSC Ensembl
Outerchr16:8442813..8559967hg38UCSC Ensembl
Innerchr16:8493818..8608537hg19UCSC Ensembl
Outerchr16:8492815..8609969hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38117155
hg19117155
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010484
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155226
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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