A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv536



Internal ID15550161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:126163548..126207710hg38UCSC Ensembl
Outerchr11:126033443..126077605hg19UCSC Ensembl
Outerchr11:125538653..125582815hg18UCSC Ensembl
Outerchr11:125538653..125582815hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3844163
hg1944163
hg1844163
hg1744163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997
SamplesNA12878
Known GenesRPUSD4
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)nsv536
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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