A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8981



Internal ID15188197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:130426088..130460248hg38UCSC Ensembl
Outerchr11:130295983..130330143hg19UCSC Ensembl
Outerchr11:129801193..129835353hg18UCSC Ensembl
Outerchr11:129801193..129835353hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg385272
hg195272
hg185272
hg175272
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550
Supporting Variants
SamplesNA12156
Known GenesADAMTS15, ADAMTS8
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)nssv8981
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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