A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519277



Internal ID15446570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:12053630..12102821hg38UCSC Ensembl
Innerchr3:12095130..12144321hg19UCSC Ensembl
Innerchr3:12070130..12119321hg18UCSC Ensembl
Innerchr3:12070130..12119321hg17UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3849192
hg1949192
hg1849192
hg1749192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699337, nssv661109, nssv674278, nssv655185
Samples
Known GenesSYN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519277
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer