A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv783384



Internal ID15730654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:106696291..106711896hg38UCSC Ensembl
Innerchr11:106567017..106582622hg19UCSC Ensembl
Innerchr11:106072227..106087832hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3815606
hg1915606
hg1815606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556229
Supporting Variants
Samples
Known GenesGUCY1A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv783384
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