A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv780241



Internal ID16074197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:87235982..87290850hg38UCSC Ensembl
Innerchr11:86947024..87001892hg19UCSC Ensembl
Innerchr11:86624672..86679540hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3854869
hg1954869
hg1854869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555710
Supporting Variants
Samples
Known GenesTMEM135
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv780241
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