A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563535



Internal ID16350944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18223945..18529572hg38UCSC Ensembl
Innerchr14:19000422..19306049hg19UCSC Ensembl
Innerchr14:18070422..18376049hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38305628
hg19305628
hg18305628
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv821197
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563535
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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