A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv863698



Internal ID15810968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89906008..89909816hg38UCSC Ensembl
Innerchr16:89972416..89976224hg19UCSC Ensembl
Innerchr16:88499917..88503725hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg383809
hg193809
hg183809
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573813
Supporting Variants
Samples
Known GenesTCF25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv863698
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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