A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7686



Internal ID15552720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:15035663..15070346hg38UCSC Ensembl
Outerchr11:15057209..15091892hg19UCSC Ensembl
Outerchr11:15013785..15048468hg18UCSC Ensembl
Outerchr11:15013785..15048468hg17UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg385330
hg195330
hg185330
hg175330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2859
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)nsv7686
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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