A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv781994



Internal ID15729264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:101038455..101042005hg38UCSC Ensembl
Innerchr11:100909186..100912736hg19UCSC Ensembl
Innerchr11:100414396..100417946hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg383551
hg193551
hg183551
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556130
Supporting Variants
Samples
Known GenesPGR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv781994
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