A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv440



Internal ID15549105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93612372..93644310hg38UCSC Ensembl
Outerchr11:93345538..93377476hg19UCSC Ensembl
Outerchr11:92985186..93017124hg18UCSC Ensembl
Outerchr11:92985186..93017124hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg388079
hg198079
hg188079
hg178079
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1953
SamplesNA18555
Known Genes
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)nsv440
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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