A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149297



Internal ID15875236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78654247..78827482hg38UCSC Ensembl
Innerchr16:78688144..78861379hg19UCSC Ensembl
Innerchr16:77245645..77418880hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38173236
hg19173236
hg18173236
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573266
Supporting Variants
SamplesHGDP00655
Known GenesWWOX
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149297
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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