A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893638



Internal ID19184458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4084575..4098215hg38UCSC Ensembl
Outerchr3:4084575..4098215hg38UCSC Ensembl
Innerchr3:4126259..4139899hg19UCSC Ensembl
Outerchr3:4126259..4139899hg19UCSC Ensembl
Innerchr3:4101259..4114899hg18UCSC Ensembl
Outerchr3:4101259..4114899hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3813641
hg1913641
hg1813641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25801311
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893638
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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