A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525368



Internal ID15105975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:186647354..186647520hg38UCSC Ensembl
Innerchr3:186365143..186365309hg19UCSC Ensembl
Innerchr3:187847837..187848003hg18UCSC Ensembl
Innerchr3:187847845..187848011hg17UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38167
hg19167
hg18167
hg17167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701488
Samples
Known GenesFETUB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525368
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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