A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv861918



Internal ID15809188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80986788..81073339hg38UCSC Ensembl
Innerchr16:81020393..81106944hg19UCSC Ensembl
Innerchr16:79577894..79664445hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3886552
hg1986552
hg1886552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573338
Supporting Variants
Samples
Known GenesATMIN, C16orf46, CENPN, CMC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv861918
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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