A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590469



Internal ID18542064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4104499..4295321hg38UCSC Ensembl
Innerchr3:4146183..4337005hg19UCSC Ensembl
Innerchr3:4121183..4312005hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38190823
hg19190823
hg18190823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002648
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3590469
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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