A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7639



Internal ID15552668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1428007..1448490hg38UCSC Ensembl
Outerchr11:1449237..1469720hg19UCSC Ensembl
Outerchr11:1405813..1426296hg18UCSC Ensembl
Outerchr11:1405813..1426296hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3820484
hg1920484
hg1820484
hg1720484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1918
SamplesNA18555
Known GenesBRSK2
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)nsv7639
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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