A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564150



Internal ID16351559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28090906..28131109hg38UCSC Ensembl
Innerchr14:28560112..28600315hg19UCSC Ensembl
Innerchr14:27629863..27670066hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3840204
hg1940204
hg1840204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv825090
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564150
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer