A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149314



Internal ID15531921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81046761..81061486hg38UCSC Ensembl
Innerchr16:81080366..81095091hg19UCSC Ensembl
Innerchr16:79637867..79652592hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3814726
hg1914726
hg1814726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573346
Supporting Variants
SamplesHGDP01232
Known GenesATMIN, C16orf46
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149314
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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