A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014667



Internal ID19103884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..63403hg38UCSC Ensembl
Innerchr3:60333..105086hg19UCSC Ensembl
Innerchr3:35333..80086hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3844749
hg1944754
hg1844754
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4602n100
Supporting Variantsnssv3593508
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)nsv1014667
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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