A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv396



Internal ID15201935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:76959072..76991701hg38UCSC Ensembl
Outerchr11:76670116..76702745hg19UCSC Ensembl
Outerchr11:76347764..76380393hg18UCSC Ensembl
Outerchr11:76347764..76380393hg17UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3832630
hg1932630
hg1832630
hg1732630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5367
SamplesNA19129
Known GenesACER3
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)nsv396
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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