A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3561553



Internal ID18762629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18714362..18714628hg38UCSC Ensembl
Outerchr3:18714302..18714681hg38UCSC Ensembl
Innerchr3:18755854..18756120hg19UCSC Ensembl
Outerchr3:18755794..18756173hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9760300
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3561553
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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