A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761270



Internal ID18735516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:128711467..128713818hg38UCSC Ensembl
Outerchr3:128711423..128714021hg38UCSC Ensembl
Innerchr3:128430310..128432661hg19UCSC Ensembl
Outerchr3:128430266..128432864hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg382599
hg192599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3562523
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761270
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