A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161276



Internal ID8252853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:161524601..161708144hg38UCSC Ensembl
Innerchr3:161242389..161425932hg19UCSC Ensembl
Innerchr3:162725083..162908626hg18UCSC Ensembl
Innerchr3:162725091..162908634hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38183544
hg19183544
hg18183544
hg17183544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422309
Supporting Variants
SamplesND03970
Known Genes
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161276
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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