A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv402



Internal ID15548687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:79573224..79617933hg38UCSC Ensembl
Outerchr11:79284268..79328977hg19UCSC Ensembl
Outerchr11:78961916..79006625hg18UCSC Ensembl
Outerchr11:78961916..79006625hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3844710
hg1944710
hg1844710
hg1744710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8937
SamplesNA12156
Known Genes
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)nsv402
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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