A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8959



Internal ID15188219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:107646652..107680407hg38UCSC Ensembl
Outerchr11:107517378..107551133hg19UCSC Ensembl
Outerchr11:107022588..107056343hg18UCSC Ensembl
Outerchr11:107022588..107056343hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg385684
hg195684
hg185684
hg175684
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv476
Supporting Variants
SamplesNA12156
Known GenesELMOD1
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)nssv8959
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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