A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9760237



Internal ID18734483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:12862514..12873001hg38UCSC Ensembl
Outerchr3:12862420..12874291hg38UCSC Ensembl
Innerchr3:12904013..12914500hg19UCSC Ensembl
Outerchr3:12903919..12915790hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3811872
hg1911872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3561490
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9760237
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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