A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564766



Internal ID16352175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:47017433..47052286hg38UCSC Ensembl
Innerchr14:47486636..47521489hg19UCSC Ensembl
Innerchr14:46556386..46591239hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3834854
hg1934854
hg1834854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3702n54
Supporting Variantsnssv827699
Samples
Known GenesMDGA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564766
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