A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3596276



Internal ID18894557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:86655021..86746299hg38UCSC Ensembl
Innerchr3:86704171..86795449hg19UCSC Ensembl
Innerchr3:86786861..86878139hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3891279
hg1991279
hg1891279
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999877
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)nssv3596276
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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