A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv853103



Internal ID15800373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21587804..21855026hg38UCSC Ensembl
Innerchr16:21599125..21866347hg19UCSC Ensembl
Innerchr16:21506626..21773848hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38267223
hg19267223
hg18267223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571631
Supporting Variants
Samples
Known GenesIGSF6, METTL9, OTOA, RRN3P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv853103
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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