A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590477



Internal ID18542072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4123660..4231805hg38UCSC Ensembl
Innerchr3:4165344..4273489hg19UCSC Ensembl
Innerchr3:4140344..4248489hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38108146
hg19108146
hg18108146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008220
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)nssv3590477
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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