A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9766140



Internal ID18740386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:21825770..21833984hg38UCSC Ensembl
Outerchr6:21824770..21834769hg38UCSC Ensembl
Innerchr6:21826001..21834215hg19UCSC Ensembl
Outerchr6:21825001..21835000hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3810000
hg1910000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3567393
Supporting Variants
Samples
Known GenesCASC15
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9766140
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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