A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011721



Internal ID22073352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21503753..21588178hg38UCSC Ensembl
Outerchr16:21401082..21590407hg38UCSC Ensembl
Innerchr16:21515074..21599499hg19UCSC Ensembl
Outerchr16:21412403..21601728hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38189326
hg19189326
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155278
Supporting Variants
Samples
Known GenesLOC100190986, LOC100271836, NPIPB3, SLC7A5P2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011721
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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