A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv371



Internal ID15548346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:68114506..68124026hg38UCSC Ensembl
Outerchr11:67881973..67891493hg19UCSC Ensembl
Outerchr11:67638549..67648069hg18UCSC Ensembl
Outerchr11:67638549..67648069hg17UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg389521
hg199521
hg189521
hg179521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8927
SamplesNA12156
Known GenesCHKA
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)nsv371
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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