A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014671



Internal ID19103888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:67857920..67935795hg38UCSC Ensembl
Innerchr3:67908344..67986219hg19UCSC Ensembl
Innerchr3:67991034..68068909hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3877876
hg1977876
hg1877876
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593969
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)nsv1014671
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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