A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526089



Internal ID15106696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:138387856..138403939hg38UCSC Ensembl
Innerchr3:138106698..138122781hg19UCSC Ensembl
Innerchr3:139589388..139605471hg18UCSC Ensembl
Innerchr3:139589396..139605479hg17UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3816084
hg1916084
hg1816084
hg1716084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702335
Samples
Known GenesMRAS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526089
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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