A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563762



Internal ID16351171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19728059..19956892hg38UCSC Ensembl
Innerchr14:20196218..20425051hg19UCSC Ensembl
Innerchr14:19266058..19494891hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38228834
hg19228834
hg18228834
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3520n54
Supporting Variantsnssv821598, nssv821599, nssv821597
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)nsv563762
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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