A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8980



Internal ID15534884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:129746107..129779495hg38UCSC Ensembl
Outerchr11:129616002..129649390hg19UCSC Ensembl
Outerchr11:129121212..129154600hg18UCSC Ensembl
Outerchr11:129121212..129154600hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg386021
hg196021
hg186021
hg176021
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548
Supporting Variants
SamplesNA12156
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)nssv8980
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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