A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565970



Internal ID16006693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103089160..103139470hg38UCSC Ensembl
Innerchr14:103555497..103605807hg19UCSC Ensembl
Innerchr14:102625250..102675560hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3850311
hg1950311
hg1850311
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834317
Samples
Known GenesEXOC3L4, TNFAIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565970
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