A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv779328



Internal ID16073284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81182270..81307644hg38UCSC Ensembl
Innerchr11:80893313..81018687hg19UCSC Ensembl
Innerchr11:80570961..80696335hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38125375
hg19125375
hg18125375
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555478
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)nssv779328
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