A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778631



Internal ID15725901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:68666713..68683779hg38UCSC Ensembl
Innerchr11:68434181..68451247hg19UCSC Ensembl
Innerchr11:68190757..68207823hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3817067
hg1917067
hg1817067
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555295
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)nssv778631
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