A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566011



Internal ID16353420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103521888..103523420hg38UCSC Ensembl
Innerchr14:103988225..103989757hg19UCSC Ensembl
Innerchr14:103057978..103059510hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381533
hg191533
hg181533
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3943n54
Supporting Variantsnssv834377
Samples
Known GenesCKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566011
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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