A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155279



Internal ID22085784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21503753..21591309hg38UCSC Ensembl
Outerchr16:21401082..21594646hg38UCSC Ensembl
Innerchr16:21515074..21602630hg19UCSC Ensembl
Outerchr16:21412403..21605967hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38193565
hg19193565
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv110n97
Supporting Variantsnssv4011723
Samples
Known GenesLOC100190986, LOC100271836, NPIPB3, SLC7A5P2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155279
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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