A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv967756



Internal ID16261712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:90209154..90315787hg38UCSC Ensembl
Innerchr3:90258304..90364937hg19UCSC Ensembl
Innerchr3:90340994..90447627hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38106634
hg19106634
hg18106634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590971
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)nssv967756
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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