A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522881



Internal ID15103488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:33694634..34200194hg38UCSC Ensembl
Innerchr3:33736126..34241686hg19UCSC Ensembl
Innerchr3:33711130..34216690hg18UCSC Ensembl
Innerchr3:33711130..34216690hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38505561
hg19505561
hg18505561
hg17505561
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698537
Samples
Known GenesCLASP2, PDCD6IP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522881
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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