A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8891



Internal ID15188287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:27050452..27059150hg38UCSC Ensembl
Outerchr11:27071999..27080697hg19UCSC Ensembl
Outerchr11:27028575..27037273hg18UCSC Ensembl
Outerchr11:27028575..27037273hg17UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg388699
hg198699
hg188699
hg178699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7720
Supporting Variants
SamplesNA12156
Known GenesBBOX1
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)nssv8891
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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