A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768328



Internal ID15715598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17537471..17577546hg38UCSC Ensembl
Innerchr11:17559018..17599093hg19UCSC Ensembl
Innerchr11:17515594..17555669hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3840076
hg1940076
hg1840076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553586
Supporting Variants
Samples
Known GenesOTOG, USH1C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv768328
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