A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3561572



Internal ID18762648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:20973168..20977235hg38UCSC Ensembl
Outerchr3:20973162..20977319hg38UCSC Ensembl
Innerchr3:21014660..21018727hg19UCSC Ensembl
Outerchr3:21014654..21018811hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg384158
hg194158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9760319
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3561572
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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