A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525296



Internal ID15452589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:126614957..126621111hg38UCSC Ensembl
Innerchr3:126333800..126339954hg19UCSC Ensembl
Innerchr3:127816490..127822644hg18UCSC Ensembl
Innerchr3:127816498..127822652hg17UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg386155
hg196155
hg186155
hg176155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701402
Samples
Known GenesTXNRD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525296
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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