A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv967752



Internal ID16261708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89930745..90150609hg38UCSC Ensembl
Innerchr3:89979895..90199759hg19UCSC Ensembl
Innerchr3:90062585..90282449hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38219865
hg19219865
hg18219865
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590968
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)nssv967752
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