A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999877



Internal ID19159413
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 StatusM
Merged Variants
Supporting Variantsnssv3596276
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)nsv999877
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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