A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3544137



Internal ID18745213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:122875130..122875179hg38UCSC Ensembl
Outerchr8:122875129..122875182hg38UCSC Ensembl
Innerchr8:123887369..123887418hg19UCSC Ensembl
Outerchr8:123887368..123887421hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9742884
Samples
Known GenesZHX2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3544137
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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