A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9742526



Internal ID18716772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:84310762..84311087hg38UCSC Ensembl
Outerchr8:84310738..84311135hg38UCSC Ensembl
Innerchr8:85222997..85223322hg19UCSC Ensembl
Outerchr8:85222973..85223370hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3543779
Supporting Variants
Samples
Known GenesRALYL
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9742526
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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