A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3565915



Internal ID18420305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:93785928..93786213hg38UCSC Ensembl
Outerchr1:93785867..93786265hg38UCSC Ensembl
Innerchr1:94251484..94251769hg19UCSC Ensembl
Outerchr1:94251423..94251821hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9764662
Samples
Known GenesBCAR3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3565915
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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