A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563800



Internal ID16351209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19827190..19920245hg38UCSC Ensembl
Innerchr14:20295349..20388404hg19UCSC Ensembl
Innerchr14:19365189..19458244hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3893056
hg1993056
hg1893056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3528n54
Supporting Variantsnssv821693
Samples
Known GenesOR4K2, OR4N2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563800
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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