A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563804



Internal ID16351213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19843929..19929208hg38UCSC Ensembl
Innerchr14:20312088..20397367hg19UCSC Ensembl
Innerchr14:19381928..19467207hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3885280
hg1985280
hg1885280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3528n54
Supporting Variantsnssv821697
Samples
Known GenesOR4K2, OR4K5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563804
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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