A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3411



Internal ID15201332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:49000067..49033342hg38UCSC Ensembl
Outerchr20:47616604..47649879hg19UCSC Ensembl
Outerchr20:47050011..47083286hg18UCSC Ensembl
Outerchr20:47050011..47083286hg17UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg386747
hg196747
hg186747
hg176747
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2338
SamplesNA18555
Known GenesARFGEF2
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)nsv3411
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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