A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564456



Internal ID16351865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40366670..40411636hg38UCSC Ensembl
Innerchr14:40835874..40880840hg19UCSC Ensembl
Innerchr14:39905624..39950590hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3844967
hg1944967
hg1844967
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv826658
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564456
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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