A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv821711



Internal ID15768981
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 StatusS
Merged Variantsnsv563812
Supporting Variants
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)nssv821711
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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