A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520682



Internal ID15447975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:153350014..153368037hg38UCSC Ensembl
Innerchr3:153067803..153085826hg19UCSC Ensembl
Innerchr3:154550493..154568516hg18UCSC Ensembl
Innerchr3:154550501..154568524hg17UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3818024
hg1918024
hg1818024
hg1718024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv690552, nssv689721, nssv674029, nssv687668
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520682
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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