A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521796



Internal ID15102403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3038825..3151219hg38UCSC Ensembl
Innerchr3:3080509..3192903hg19UCSC Ensembl
Innerchr3:3055509..3167903hg18UCSC Ensembl
Innerchr3:3055509..3167903hg17UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38112395
hg19112395
hg18112395
hg17112395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694098
Samples
Known GenesCNTN4, CRBN, IL5RA, TRNT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521796
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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