A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3557027



Internal ID18758103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:35033868..35034161hg38UCSC Ensembl
Outerchr20:35033802..35034224hg38UCSC Ensembl
Innerchr20:33621671..33621964hg19UCSC Ensembl
Outerchr20:33621605..33622027hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9755774
Samples
Known GenesTRPC4AP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3557027
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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