A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3386



Internal ID15547990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:44059803..44073580hg38UCSC Ensembl
Outerchr20:42688443..42702220hg19UCSC Ensembl
Outerchr20:42121857..42135634hg18UCSC Ensembl
Outerchr20:42121857..42135634hg17UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3813778
hg1913778
hg1813778
hg1713778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7683
SamplesNA12156
Known GenesTOX2
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)nsv3386
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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