A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv853099



Internal ID15800369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21563897..21728953hg38UCSC Ensembl
Innerchr16:21575218..21740274hg19UCSC Ensembl
Innerchr16:21482719..21647775hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38165057
hg19165057
hg18165057
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571628
Supporting Variants
Samples
Known GenesIGSF6, METTL9, OTOA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv853099
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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