A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563775



Internal ID16351184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19745778..19955706hg38UCSC Ensembl
Innerchr14:20213937..20423865hg19UCSC Ensembl
Innerchr14:19283777..19493705hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38209929
hg19209929
hg18209929
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3520n54
Supporting Variantsnssv821657
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)nsv563775
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