A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8940



Internal ID15534924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:80686644..80724447hg38UCSC Ensembl
Outerchr11:80397688..80435490hg19UCSC Ensembl
Outerchr11:80075336..80113138hg18UCSC Ensembl
Outerchr11:80075336..80113138hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3837804
hg1937803
hg1837803
hg1737803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv408
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)nssv8940
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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