A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953654



Internal ID16955841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:45628387..45643786hg38UCSC Ensembl
Outerchr21:47048301..47063700hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3815400
hg1915400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000705
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953654
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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