A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590189



Internal ID18541784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..104362hg38UCSC Ensembl
Innerchr3:60333..146045hg19UCSC Ensembl
Innerchr3:35333..121045hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3885708
hg1985713
hg1885713
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004219
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)nssv3590189
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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