A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4010484



Internal ID22072115
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 Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155226
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4010484
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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