A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778915



Internal ID15726185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:70156780..70248052hg38UCSC Ensembl
Innerchr11:70002886..70094158hg19UCSC Ensembl
Innerchr11:69680534..69771806hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3891273
hg1991273
hg1891273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555376
Supporting Variants
Samples
Known GenesANO1, FADD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778915
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