A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525295



Internal ID15452588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:35481219..35538367hg38UCSC Ensembl
Innerchr21:36853517..36910664hg19UCSC Ensembl
Innerchr21:35775387..35832534hg18UCSC Ensembl
Innerchr21:35775387..35832534hg17UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3857149
hg1957148
hg1857148
hg1757148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701401
Samples
Known GenesLOC100506403
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525295
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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