A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054426



Internal ID18796957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:466922..546442hg38UCSC Ensembl
Innerchr16:516922..596442hg19UCSC Ensembl
Innerchr16:456923..536443hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3879521
hg1979521
hg1879521
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3556944
Samples
Known GenesCAPN15, LINC00235, MIR3176, MIR5587, RAB11FIP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054426
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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