A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3063



Internal ID15540912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:24035294..24069205hg38UCSC Ensembl
Outerchr20:24015931..24049842hg19UCSC Ensembl
Outerchr20:23963931..23997842hg18UCSC Ensembl
Outerchr20:23963931..23997842hg17UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg386112
hg196112
hg186112
hg176112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3337
Supporting Variants
SamplesNA18555
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)nssv3063
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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