A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852290



Internal ID16146246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4015582..4037975hg38UCSC Ensembl
Innerchr16:4065583..4087976hg19UCSC Ensembl
Innerchr16:4005584..4027977hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3822394
hg1922394
hg1822394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571271
Supporting Variants
Samples
Known GenesADCY9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852290
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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