A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566004



Internal ID16353413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103521722..103523689hg38UCSC Ensembl
Innerchr14:103988059..103990026hg19UCSC Ensembl
Innerchr14:103057812..103059779hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381968
hg191968
hg181968
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834370
Samples
Known GenesCKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566004
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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