A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1481



Internal ID15199358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:32635939..32642395hg38UCSC Ensembl
Outerchr15:32928140..32934596hg19UCSC Ensembl
Outerchr15:30715432..30721888hg18UCSC Ensembl
Outerchr15:30715432..30721888hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg386457
hg196457
hg186457
hg176457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7154
SamplesNA12156
Known GenesARHGAP11A, SCG5
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)nsv1481
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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