A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761692



Internal ID18735938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176334017..176335015hg38UCSC Ensembl
Outerchr3:176333764..176335204hg38UCSC Ensembl
Innerchr3:176051805..176052803hg19UCSC Ensembl
Outerchr3:176051552..176052992hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg381441
hg191441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3562945
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761692
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