A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590226



Internal ID18541821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24337..104040hg38UCSC Ensembl
Innerchr3:66011..145723hg19UCSC Ensembl
Innerchr3:41011..120723hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3879704
hg1979713
hg1879713
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997453
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)nssv3590226
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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