A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3408



Internal ID15548014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:48854855..48893289hg38UCSC Ensembl
Outerchr20:47471392..47509826hg19UCSC Ensembl
Outerchr20:46904799..46943233hg18UCSC Ensembl
Outerchr20:46904799..46943233hg17UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3838435
hg1938435
hg1838435
hg1738435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7691
SamplesNA12156
Known Genes
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)nsv3408
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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