A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526609



Internal ID15453902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43063662..43067294hg38UCSC Ensembl
Innerchr21:44483772..44487404hg19UCSC Ensembl
Innerchr21:43356841..43360473hg18UCSC Ensembl
Innerchr21:43356841..43360473hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg383633
hg193633
hg183633
hg173633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702929
Samples
Known GenesCBS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526609
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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