A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526395



Internal ID15453688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:35492159..35523898hg38UCSC Ensembl
Innerchr21:36864457..36896196hg19UCSC Ensembl
Innerchr21:35786327..35818066hg18UCSC Ensembl
Innerchr21:35786327..35818066hg17UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3831740
hg1931740
hg1831740
hg1731740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702694
Samples
Known GenesLOC100506403
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526395
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer