A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564075



Internal ID16351484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:25810345..25821843hg38UCSC Ensembl
Innerchr14:26279551..26291049hg19UCSC Ensembl
Innerchr14:25349391..25360889hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3811499
hg1911499
hg1811499
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3584n54
Supporting Variantsnssv824521
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564075
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