A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526908



Internal ID15454201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41318043..41744517hg38UCSC Ensembl
Innerchr3:41359534..41786009hg19UCSC Ensembl
Innerchr3:41334538..41761013hg18UCSC Ensembl
Innerchr3:41334538..41761013hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38426475
hg19426476
hg18426476
hg17426476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703268
Samples
Known GenesULK4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526908
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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