A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3596229



Internal ID18547824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:80076768..80432936hg38UCSC Ensembl
Innerchr3:80125918..80482086hg19UCSC Ensembl
Innerchr3:80208608..80564776hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38356169
hg19356169
hg18356169
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012046
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)nssv3596229
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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