A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv449



Internal ID15549204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:95456535..95487558hg38UCSC Ensembl
Outerchr11:95189699..95220722hg19UCSC Ensembl
Outerchr11:94829347..94860370hg18UCSC Ensembl
Outerchr11:94829347..94860370hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg388487
hg198487
hg188487
hg178487
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10834
SamplesNA18956
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)nsv449
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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