A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565579



Internal ID16352988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:93987862..93988969hg38UCSC Ensembl
Innerchr14:94454208..94455315hg19UCSC Ensembl
Innerchr14:93523961..93525068hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg381108
hg191108
hg181108
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3854n54
Supporting Variantsnssv832440
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565579
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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