A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7691



Internal ID15552726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:17130046..17175347hg38UCSC Ensembl
Outerchr11:17151593..17196894hg19UCSC Ensembl
Outerchr11:17108169..17153470hg18UCSC Ensembl
Outerchr11:17108169..17153470hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3845302
hg1945302
hg1845302
hg1745302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8885
SamplesNA12156
Known GenesPIK3C2A
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)nsv7691
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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