A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9765876



Internal ID18393436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:666619..667645hg38UCSC Ensembl
Outerchr6:666318..667883hg38UCSC Ensembl
Innerchr6:666619..667645hg19UCSC Ensembl
Outerchr6:666318..667883hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381566
hg191566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3567129
Supporting Variants
Samples
Known GenesEXOC2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9765876
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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