A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10836



Internal ID15195276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:102922044..102954570hg38UCSC Ensembl
Outerchr11:102792774..102825299hg19UCSC Ensembl
Outerchr11:102297984..102330509hg18UCSC Ensembl
Outerchr11:102297984..102330509hg17UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg386984
hg196984
hg186984
hg176984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv464
Supporting Variants
SamplesNA18956
Known GenesMMP13
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)nssv10836
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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