A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv821597



Internal ID16115553
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 StatusS
Merged Variantsnsv563762
Supporting Variants
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)nssv821597
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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