A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2855



Internal ID15541706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1749402..1782951hg38UCSC Ensembl
Outerchr11:1770632..1804181hg19UCSC Ensembl
Outerchr11:1727208..1760757hg18UCSC Ensembl
Outerchr11:1727208..1760757hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg386482
hg196482
hg186482
hg176482
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7642
Supporting Variants
SamplesNA18555
Known GenesCTSD, IFITM10, MOB2
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)nssv2855
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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