A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590197



Internal ID18541792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..110923hg38UCSC Ensembl
Innerchr3:60333..152606hg19UCSC Ensembl
Innerchr3:35333..127606hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3892269
hg1992274
hg1892274
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014700
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)nssv3590197
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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