A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517831



Internal ID15098438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:11541780..11576994hg38UCSC Ensembl
Innerchr3:11583254..11618468hg19UCSC Ensembl
Innerchr3:11558254..11593468hg18UCSC Ensembl
Innerchr3:11558254..11593468hg17UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3835215
hg1935215
hg1835215
hg1735215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695235
Samples
Known GenesATG7, VGLL4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517831
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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