A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571273



Internal ID16358682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4115431..4116813hg38UCSC Ensembl
Innerchr16:4165432..4166814hg19UCSC Ensembl
Innerchr16:4105433..4106815hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381383
hg191383
hg181383
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852296, nssv852297, nssv852294, nssv852293, nssv852299, nssv852300, nssv852295, nssv852292, nssv852298
Samples
Known GenesADCY9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571273
Frequency
Sample Size17421
Observed Gain8
Observed Loss1
Observed Complex0
Frequencyn/a


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