A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761876



Internal ID18736122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:194634862..194635945hg38UCSC Ensembl
Outerchr3:194634591..194636071hg38UCSC Ensembl
Innerchr3:194355591..194356674hg19UCSC Ensembl
Outerchr3:194355320..194356800hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381481
hg191481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3563129
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761876
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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