A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv463



Internal ID8516340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:102740254..102773199hg38UCSC Ensembl
Outerchr11:102610985..102643930hg19UCSC Ensembl
Outerchr11:102116195..102149140hg18UCSC Ensembl
Outerchr11:102116195..102149140hg17UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg387050
hg197050
hg187050
hg177050
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1959
SamplesNA18555
Known GenesMMP10
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)nsv463
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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