A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852008



Internal ID15799278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1364660..1374128hg38UCSC Ensembl
Innerchr16:1414661..1424129hg19UCSC Ensembl
Innerchr16:1354662..1364130hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg389469
hg199469
hg189469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571144
Supporting Variants
Samples
Known GenesUNKL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852008
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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