A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3329



Internal ID15547927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:21804370..21817961hg38UCSC Ensembl
Outerchr20:21785008..21798599hg19UCSC Ensembl
Outerchr20:21733008..21746599hg18UCSC Ensembl
Outerchr20:21733008..21746599hg17UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg389270
hg199270
hg189270
hg179270
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2330
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)nsv3329
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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