A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518352



Internal ID15098959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8905994..9089915hg38UCSC Ensembl
Innerchr3:8947678..9131599hg19UCSC Ensembl
Innerchr3:8922678..9106599hg18UCSC Ensembl
Innerchr3:8922678..9106599hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38183922
hg19183922
hg18183922
hg17183922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695780
Samples
Known GenesRAD18, SRGAP3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518352
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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