A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3490



Internal ID15548105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:31579840..31617051hg38UCSC Ensembl
Outerchr21:32952153..32989364hg19UCSC Ensembl
Outerchr21:31874024..31911235hg18UCSC Ensembl
Outerchr21:31874024..31911235hg17UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3837212
hg1937212
hg1837212
hg1737212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7713
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)nsv3490
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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