A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755774



Internal ID18730020
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 StatusS
Merged Variantsesv3557027
Supporting Variants
Samples
Known GenesTRPC4AP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755774
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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