A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv783619



Internal ID15730889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:106915897..106917261hg38UCSC Ensembl
Innerchr11:106786623..106787987hg19UCSC Ensembl
Innerchr11:106291833..106293197hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381365
hg191365
hg181365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556249
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)nssv783619
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