A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155288



Internal ID22085793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:22546611..22701658hg38UCSC Ensembl
Outerchr16:22430699..22706267hg38UCSC Ensembl
Innerchr16:22557932..22712979hg19UCSC Ensembl
Outerchr16:22442020..22717588hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38275569
hg19275569
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv111n97
Supporting Variantsnssv4012471, nssv4012472
Samples
Known GenesLOC653786, NPIPB5, RRN3P3, SMG1P1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155288
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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