A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3557023



Internal ID18411413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:34654459..34656057hg38UCSC Ensembl
Outerchr20:34653871..34656493hg38UCSC Ensembl
Innerchr20:33242263..33243861hg19UCSC Ensembl
Outerchr20:33241675..33244297hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg382623
hg192623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9755770
Samples
Known GenesPIGU
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3557023
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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