A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3561638



Internal ID18762714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26544165..26547052hg38UCSC Ensembl
Outerchr3:26543943..26547320hg38UCSC Ensembl
Innerchr3:26585656..26588543hg19UCSC Ensembl
Outerchr3:26585434..26588811hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg383378
hg193378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9760385
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3561638
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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