A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3451



Internal ID15201376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:10395590..10420993hg38UCSC Ensembl
Outerchr21:11091464..11116867hg19UCSC Ensembl
Outerchr21:10113335..10138738hg18UCSC Ensembl
Outerchr21:10113335..10138738hg17UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3811888
hg1911888
hg1811888
hg1711888
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1615
SamplesNA19240
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5
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)nsv3451
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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