A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705647



Internal ID15095613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:27362643..27363079hg38UCSC Ensembl
Innerchr16:27373964..27374400hg19UCSC Ensembl
Innerchr16:27281465..27281901hg18UCSC Ensembl
Innerchr16:27281465..27281901hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38437
hg19437
hg18437
hg17437
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516053
Supporting Variants
Samples
Known GenesIL4R
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705647
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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