A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518089



Internal ID15445382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:135502662..135514152hg38UCSC Ensembl
Innerchr3:135221504..135232994hg19UCSC Ensembl
Innerchr3:136704194..136715684hg18UCSC Ensembl
Innerchr3:136704202..136715692hg17UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3811491
hg1911491
hg1811491
hg1711491
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695502
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518089
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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