A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv863632



Internal ID15810902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89852186..89852908hg38UCSC Ensembl
Innerchr16:89918594..89919316hg19UCSC Ensembl
Innerchr16:88446095..88446817hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38723
hg19723
hg18723
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573797
Supporting Variants
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv863632
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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