A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8914



Internal ID15188264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:57765169..57783274hg38UCSC Ensembl
Outerchr11:57532641..57550746hg19UCSC Ensembl
Outerchr11:57289217..57307322hg18UCSC Ensembl
Outerchr11:57289217..57307322hg17UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3818106
hg1918106
hg1818106
hg1718106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv327
Supporting Variants
SamplesNA12156
Known GenesCTNND1, TMX2-CTNND1
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)nssv8914
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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