A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893632



Internal ID18837766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4319799..4378571hg38UCSC Ensembl
Outerchr3:4315301..4378571hg38UCSC Ensembl
Innerchr3:4361483..4420255hg19UCSC Ensembl
Outerchr3:4356985..4420255hg19UCSC Ensembl
Innerchr3:4336483..4395255hg18UCSC Ensembl
Outerchr3:4331985..4395255hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3863271
hg1963271
hg1863271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783100, essv25801180
Samples
Known GenesSETMAR, SUMF1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893632
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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