A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563846



Internal ID16351255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20376700..20386079hg38UCSC Ensembl
Innerchr14:20844859..20854238hg19UCSC Ensembl
Innerchr14:19914699..19924078hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg389380
hg199380
hg189380
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv823016
Samples
Known GenesTEP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563846
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