A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519313



Internal ID15099920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:10480994..10483503hg38UCSC Ensembl
Innerchr3:10522678..10525187hg19UCSC Ensembl
Innerchr3:10497678..10500187hg18UCSC Ensembl
Innerchr3:10497678..10500187hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg382510
hg192510
hg182510
hg172510
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696786
Samples
Known GenesATP2B2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519313
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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