A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563783



Internal ID16351192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19750966..19776378hg38UCSC Ensembl
Innerchr14:20219125..20244537hg19UCSC Ensembl
Innerchr14:19288965..19314377hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3825413
hg1925413
hg1825413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3525n54
Supporting Variantsnssv821671
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563783
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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