A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563784



Internal ID16351193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19750966..19779621hg38UCSC Ensembl
Innerchr14:20219125..20247780hg19UCSC Ensembl
Innerchr14:19288965..19317620hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3828656
hg1928656
hg1828656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3525n54
Supporting Variantsnssv821672
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563784
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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