A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590484



Internal ID18542079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4125592..4271801hg38UCSC Ensembl
Innerchr3:4167276..4313485hg19UCSC Ensembl
Innerchr3:4142276..4288485hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38146210
hg19146210
hg18146210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008570
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)nssv3590484
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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