A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852334



Internal ID16146290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4315622..4317220hg38UCSC Ensembl
Innerchr16:4365623..4367221hg19UCSC Ensembl
Innerchr16:4305624..4307222hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381599
hg191599
hg181599
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571298
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852334
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