A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524086



Internal ID15451379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113536325..113546147hg38UCSC Ensembl
Innerchr3:113255172..113264994hg19UCSC Ensembl
Innerchr3:114737862..114747684hg18UCSC Ensembl
Innerchr3:114737862..114747684hg17UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg389823
hg199823
hg189823
hg179823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699956
Samples
Known GenesSIDT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524086
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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