A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv860934



Internal ID16154890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78216158..78318860hg38UCSC Ensembl
Innerchr16:78250055..78352757hg19UCSC Ensembl
Innerchr16:76807556..76910258hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38102703
hg19102703
hg18102703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573142
Supporting Variants
Samples
Known GenesWWOX
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv860934
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer