A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7688



Internal ID15552722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:16891212..16918257hg38UCSC Ensembl
Outerchr11:16912759..16939804hg19UCSC Ensembl
Outerchr11:16869335..16896380hg18UCSC Ensembl
Outerchr11:16869335..16896380hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3827046
hg1927046
hg1827046
hg1727046
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10805
SamplesNA18956
Known GenesPLEKHA7
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)nsv7688
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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