A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv353



Internal ID15201462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:63643744..63661026hg38UCSC Ensembl
Outerchr11:63411216..63428498hg19UCSC Ensembl
Outerchr11:63167792..63185074hg18UCSC Ensembl
Outerchr11:63167792..63185074hg17UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3817283
hg1917283
hg1817283
hg1717283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8922
SamplesNA12156
Known GenesATL3
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)nsv353
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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