A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565910



Internal ID16353319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101711842..101727209hg38UCSC Ensembl
Innerchr14:102178179..102193546hg19UCSC Ensembl
Innerchr14:101247932..101263299hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3815368
hg1915368
hg1815368
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834061, nssv834063, nssv834062
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565910
Frequency
Sample Size17421
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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