A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv415



Internal ID15548830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:84213898..84258560hg38UCSC Ensembl
Outerchr11:83924941..83969603hg19UCSC Ensembl
Outerchr11:83602589..83647251hg18UCSC Ensembl
Outerchr11:83602589..83647251hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3844663
hg1944663
hg1844663
hg1744663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8942
SamplesNA12156
Known GenesDLG2
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)nsv415
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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