A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175086



Internal ID15855760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:20668471..20738448hg38UCSC Ensembl
Innerchr11:20690017..20759994hg19UCSC Ensembl
Innerchr11:20646593..20716570hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3869978
hg1969978
hg1869978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553680
Supporting Variants
Samples1782681313_A
Known GenesNELL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175086
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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