A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9742122



Internal ID18369682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:38529983..38550382hg38UCSC Ensembl
Outerchr8:38526023..38553613hg38UCSC Ensembl
Innerchr8:38387501..38407900hg19UCSC Ensembl
Outerchr8:38383541..38411131hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3827591
hg1927591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3543375
Supporting Variants
Samples
Known GenesC8orf86
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9742122
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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