A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563758



Internal ID16351167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19728059..19954442hg38UCSC Ensembl
Innerchr14:20196218..20422601hg19UCSC Ensembl
Innerchr14:19266058..19492441hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38226384
hg19226384
hg18226384
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3520n54
Supporting Variantsnssv821569
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)nsv563758
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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