A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565889



Internal ID16353298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101702580..101735235hg38UCSC Ensembl
Innerchr14:102168917..102201572hg19UCSC Ensembl
Innerchr14:101238670..101271325hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3832656
hg1932656
hg1832656
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv833739
Samples
Known GenesLINC00239
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565889
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