A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764492



Internal ID16058448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2165105..2212721hg38UCSC Ensembl
Innerchr11:2186335..2233951hg19UCSC Ensembl
Innerchr11:2142911..2190527hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3847617
hg1947617
hg1847617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553079
Supporting Variants
Samples
Known GenesMIR4686, TH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764492
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