A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852226



Internal ID16146182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:2648591..2660912hg38UCSC Ensembl
Innerchr16:2698592..2710913hg19UCSC Ensembl
Innerchr16:2638593..2650914hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3812322
hg1912322
hg1812322
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571225
Supporting Variants
Samples
Known GenesERVK13-1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852226
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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