A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564192



Internal ID16004915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34256027..34527301hg38UCSC Ensembl
Innerchr14:34725233..34996507hg19UCSC Ensembl
Innerchr14:33794984..34066258hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg38271275
hg19271275
hg18271275
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3608n54
Supporting Variantsnssv825153
Samples
Known GenesEAPP, SPTSSA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564192
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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