A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528658



Internal ID15109265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:40371712..40388490hg38UCSC Ensembl
Innerchr21:41743639..41760417hg19UCSC Ensembl
Innerchr21:40665509..40682287hg18UCSC Ensembl
Innerchr21:40665509..40682287hg17UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3816779
hg1916779
hg1816779
hg1716779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705292
Samples
Known GenesDSCAM, DSCAM-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528658
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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