A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv821626



Internal ID16115582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19734966..19977459hg38UCSC Ensembl
Innerchr14:20203125..20445618hg19UCSC Ensembl
Innerchr14:19272965..19515458hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38242494
hg19242494
hg18242494
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563773
Supporting Variants
Samples
Known GenesOR4K1, OR4K15, 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)nssv821626
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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