A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562597



Internal ID18416987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:136253468..136254543hg38UCSC Ensembl
Outerchr3:136253415..136254728hg38UCSC Ensembl
Innerchr3:135972310..135973385hg19UCSC Ensembl
Outerchr3:135972257..135973570hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg381314
hg191314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9761344
Samples
Known GenesPCCB
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562597
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