A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755817



Internal ID18383377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:41184285..41184386hg38UCSC Ensembl
Outerchr20:41184281..41184388hg38UCSC Ensembl
Innerchr20:39812925..39813026hg19UCSC Ensembl
Outerchr20:39812921..39813028hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3557070
Supporting Variants
Samples
Known GenesZHX3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755817
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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