A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893650



Internal ID19184470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6027173..6094747hg38UCSC Ensembl
Outerchr3:6027173..6094747hg38UCSC Ensembl
Innerchr3:6068860..6136434hg19UCSC Ensembl
Outerchr3:6068860..6136434hg19UCSC Ensembl
Innerchr3:6043860..6111434hg18UCSC Ensembl
Outerchr3:6043860..6111434hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3867575
hg1967575
hg1867575
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789347
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893650
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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