A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv780546



Internal ID15727816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90218342..90309371hg38UCSC Ensembl
Innerchr11:89951510..90042539hg19UCSC Ensembl
Innerchr11:89591158..89682187hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3891030
hg1991030
hg1891030
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555834
Supporting Variants
Samples
Known GenesCHORDC1, DISC1FP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv780546
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