A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv776857



Internal ID16070813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55940328..55962275hg38UCSC Ensembl
Innerchr11:55707804..55729751hg19UCSC Ensembl
Innerchr11:55464380..55486327hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3821948
hg1921948
hg1821948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555094
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv776857
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