A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563779



Internal ID16351188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19745778..19969990hg38UCSC Ensembl
Innerchr14:20213937..20438149hg19UCSC Ensembl
Innerchr14:19283777..19507989hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38224213
hg19224213
hg18224213
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3520n54
Supporting Variantsnssv821666
Samples
Known GenesOR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563779
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