A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155278



Internal ID22085783
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv110n97
Supporting Variantsnssv4011721, nssv4011722
Samples
Known GenesLOC100190986, LOC100271836, NPIPB3, SLC7A5P2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155278
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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