A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761588



Internal ID18735834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162808213..162905521hg38UCSC Ensembl
Outerchr3:162784713..162911662hg38UCSC Ensembl
Innerchr3:162526001..162623309hg19UCSC Ensembl
Outerchr3:162502501..162629450hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38126950
hg19126950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3562841
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761588
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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