A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9764662



Internal ID18392222
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 StatusS
Merged Variantsesv3565915
Supporting Variants
Samples
Known GenesBCAR3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9764662
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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