A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3557072



Internal ID18411462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:41257724..41258003hg38UCSC Ensembl
Outerchr20:41257709..41258046hg38UCSC Ensembl
Innerchr20:39886364..39886643hg19UCSC Ensembl
Outerchr20:39886349..39886686hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9755819
Samples
Known GenesZHX3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3557072
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer