A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8887



Internal ID15188291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:17535241..17580224hg38UCSC Ensembl
Outerchr11:17556788..17601771hg19UCSC Ensembl
Outerchr11:17513364..17558347hg18UCSC Ensembl
Outerchr11:17513364..17558347hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3844984
hg1944984
hg1844984
hg1744984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7693
Supporting Variants
SamplesNA12156
Known GenesOTOG, USH1C
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)nssv8887
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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