A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9742583



Internal ID18716829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:91140654..91140914hg38UCSC Ensembl
Outerchr8:91140606..91140983hg38UCSC Ensembl
Innerchr8:92152882..92153142hg19UCSC Ensembl
Outerchr8:92152834..92153211hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3543836
Supporting Variants
Samples
Known GenesLRRC69
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9742583
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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