A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3543385



Internal ID18744461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39096104..39096336hg38UCSC Ensembl
Outerchr8:39096074..39096387hg38UCSC Ensembl
Innerchr8:38953623..38953855hg19UCSC Ensembl
Outerchr8:38953593..38953906hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9742132
Samples
Known GenesADAM9
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3543385
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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