A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv780246



Internal ID16074202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:87260506..87302396hg38UCSC Ensembl
Innerchr11:86971548..87013438hg19UCSC Ensembl
Innerchr11:86649196..86691086hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3841891
hg1941891
hg1841891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555713
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)nssv780246
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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