A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564821



Internal ID16352230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48334164..48451683hg38UCSC Ensembl
Innerchr14:48803367..48920886hg19UCSC Ensembl
Innerchr14:47873117..47990636hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38117520
hg19117520
hg18117520
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3712n54
Supporting Variantsnssv827854
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564821
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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