A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564556



Internal ID16351965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:41200899..41255120hg38UCSC Ensembl
Innerchr14:41670102..41724323hg19UCSC Ensembl
Innerchr14:40739852..40794073hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3854222
hg1954222
hg1854222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3670n54
Supporting Variantsnssv827219
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564556
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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