A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7689



Internal ID15552723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:16924406..16969305hg38UCSC Ensembl
Outerchr11:16945953..16990852hg19UCSC Ensembl
Outerchr11:16902529..16947428hg18UCSC Ensembl
Outerchr11:16902529..16947428hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3844900
hg1944900
hg1844900
hg1744900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8884
SamplesNA12156
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)nsv7689
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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