A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564152



Internal ID16351561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28138868..28187540hg38UCSC Ensembl
Innerchr14:28608074..28656746hg19UCSC Ensembl
Innerchr14:27677825..27726497hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3848673
hg1948673
hg1848673
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3601n54
Supporting Variantsnssv825093, nssv825092
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564152
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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