A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852097



Internal ID16146053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:2472814..2475915hg38UCSC Ensembl
Innerchr16:2522815..2525916hg19UCSC Ensembl
Innerchr16:2462816..2465917hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg383102
hg193102
hg183102
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571207
Supporting Variants
Samples
Known GenesNTN3, TBC1D24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852097
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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