A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3563123



Internal ID18764199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:194400494..194401185hg38UCSC Ensembl
Outerchr3:194400362..194401292hg38UCSC Ensembl
Innerchr3:194121223..194121914hg19UCSC Ensembl
Outerchr3:194121091..194122021hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38931
hg19931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9761870
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3563123
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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