A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526760



Internal ID15454053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:28310232..28323668hg38UCSC Ensembl
Innerchr22:28706220..28719656hg19UCSC Ensembl
Innerchr22:27036220..27049656hg18UCSC Ensembl
Innerchr22:27030774..27044210hg17UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3813437
hg1913437
hg1813437
hg1713437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703110
Samples
Known GenesMIR548AM, TTC28
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526760
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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