A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10833



Internal ID15541965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:94760379..94790111hg38UCSC Ensembl
Outerchr11:94493545..94523277hg19UCSC Ensembl
Outerchr11:94133193..94162925hg18UCSC Ensembl
Outerchr11:94133193..94162925hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg389766
hg199766
hg189766
hg179766
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv445
Supporting Variants
SamplesNA18956
Known GenesAMOTL1
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)nssv10833
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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