A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563812



Internal ID16004535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19935932..20226809hg38UCSC Ensembl
Innerchr14:20404091..20694968hg19UCSC Ensembl
Innerchr14:19473931..19764808hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38290878
hg19290878
hg18290878
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3532n54
Supporting Variantsnssv821711
Samples
Known GenesOR11G2, OR11H6, OR4K1, OR4K13, OR4K14, OR4K15, OR4K17, OR4L1, OR4N5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563812
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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