A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852094



Internal ID16146050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:2464111..2474820hg38UCSC Ensembl
Innerchr16:2514112..2524821hg19UCSC Ensembl
Innerchr16:2454113..2464822hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3810710
hg1910710
hg1810710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571204
Supporting Variants
Samples
Known GenesC16orf59, NTN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852094
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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