A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv861691



Internal ID15808961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79124285..80093429hg38UCSC Ensembl
Innerchr16:79158182..80127326hg19UCSC Ensembl
Innerchr16:77715683..78684827hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38969145
hg19969145
hg18969145
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573285
Supporting Variants
Samples
Known GenesLOC101928248, LOC102467146, MAF, WWOX
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv861691
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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