A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519414



Internal ID15446707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8621741..8634092hg38UCSC Ensembl
Innerchr3:8663427..8675778hg19UCSC Ensembl
Innerchr3:8638427..8650778hg18UCSC Ensembl
Innerchr3:8638427..8650778hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3812352
hg1912352
hg1812352
hg1712352
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696840
Samples
Known GenesSSUH2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519414
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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