A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011606



Internal ID22073237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21503753..21575403hg38UCSC Ensembl
Outerchr16:21401082..21577467hg38UCSC Ensembl
Innerchr16:21515074..21586724hg19UCSC Ensembl
Outerchr16:21412403..21588788hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38176386
hg19176386
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155274
Supporting Variants
Samples
Known GenesLOC100190986, LOC100271836, NPIPB3, SLC7A5P2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011606
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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