A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9265



Internal ID15193530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1885616..1923433hg38UCSC Ensembl
Outerchr11:1906846..1944663hg19UCSC Ensembl
Outerchr11:1863422..1901239hg18UCSC Ensembl
Outerchr11:1863422..1901239hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3837818
hg1937818
hg1837818
hg1737818
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7643
Supporting Variants
SamplesNA18517
Known GenesLSP1, TNNT3
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)nssv9265
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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