A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8880



Internal ID15534984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:9268829..9313481hg38UCSC Ensembl
Outerchr11:9290376..9335028hg19UCSC Ensembl
Outerchr11:9246952..9291604hg18UCSC Ensembl
Outerchr11:9246952..9291604hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3844653
hg1944653
hg1844653
hg1744653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7669
Supporting Variants
SamplesNA12156
Known GenesTMEM41B
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv8880
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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