A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3916



Internal ID15191957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1876115..1917413hg38UCSC Ensembl
Outerchr11:1897345..1938643hg19UCSC Ensembl
Outerchr11:1853921..1895219hg18UCSC Ensembl
Outerchr11:1853921..1895219hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3841299
hg1941299
hg1841299
hg1741299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7643
Supporting Variants
SamplesNA12878
Known GenesLSP1
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)nssv3916
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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