A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv465



Internal ID15202694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:102926638..102971487hg38UCSC Ensembl
Outerchr11:102797367..102842216hg19UCSC Ensembl
Outerchr11:102302577..102347426hg18UCSC Ensembl
Outerchr11:102302577..102347426hg17UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3844850
hg1944850
hg1844850
hg1744850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8956
SamplesNA12156
Known GenesMMP13
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)nsv465
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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