A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522239



Internal ID15102846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4115819..4319799hg38UCSC Ensembl
Innerchr3:4157503..4361483hg19UCSC Ensembl
Innerchr3:4132503..4336483hg18UCSC Ensembl
Innerchr3:4132503..4336483hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38203981
hg19203981
hg18203981
hg17203981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv272n21
Supporting Variantsnssv695020
Samples
Known GenesSETMAR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522239
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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