A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565911



Internal ID16353320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101711842..101735235hg38UCSC Ensembl
Innerchr14:102178179..102201572hg19UCSC Ensembl
Innerchr14:101247932..101271325hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3823394
hg1923394
hg1823394
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834064, nssv834065, nssv834066
Samples
Known GenesLINC00239
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565911
Frequency
Sample Size17421
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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