A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565584



Internal ID16352993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:93987915..93988969hg38UCSC Ensembl
Innerchr14:94454261..94455315hg19UCSC Ensembl
Innerchr14:93524014..93525068hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg381055
hg191055
hg181055
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3854n54
Supporting Variantsnssv832445
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565584
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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