A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571272



Internal ID16358681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4112759..4116762hg38UCSC Ensembl
Innerchr16:4162760..4166763hg19UCSC Ensembl
Innerchr16:4102761..4106764hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg384004
hg194004
hg184004
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852291
Samples
Known GenesADCY9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571272
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer