A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893832



Internal ID19184652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:181891953..181924740hg38UCSC Ensembl
Outerchr3:181891953..181924740hg38UCSC Ensembl
Innerchr3:181609741..181642528hg19UCSC Ensembl
Outerchr3:181609741..181642528hg19UCSC Ensembl
Innerchr3:183092435..183125222hg18UCSC Ensembl
Outerchr3:183092435..183125222hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3832788
hg1932788
hg1832788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786954
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893832
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