A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3531



Internal ID15201464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:42251325..42297079hg38UCSC Ensembl
Outerchr21:43671435..43717189hg19UCSC Ensembl
Outerchr21:42544504..42590258hg18UCSC Ensembl
Outerchr21:42544504..42590258hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3845755
hg1945755
hg1845755
hg1745755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5908
SamplesNA19129
Known GenesABCG1
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)nsv3531
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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