A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4010478



Internal ID22072109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3164685..3187581hg38UCSC Ensembl
Outerchr16:3161319..3198359hg38UCSC Ensembl
Innerchr16:3214686..3237581hg19UCSC Ensembl
Outerchr16:3211320..3248359hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3837041
hg1937040
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155221
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4010478
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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