A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893810



Internal ID19184630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:168175986..168229728hg38UCSC Ensembl
Outerchr3:168175986..168229728hg38UCSC Ensembl
Innerchr3:167893774..167947516hg19UCSC Ensembl
Outerchr3:167893774..167947516hg19UCSC Ensembl
Innerchr3:169376468..169430210hg18UCSC Ensembl
Outerchr3:169376468..169430210hg18UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3853743
hg1953743
hg1853743
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787774, essv25787940
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893810
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer