A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755790



Internal ID18383350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37187219..37187506hg38UCSC Ensembl
Outerchr20:37187152..37187546hg38UCSC Ensembl
Innerchr20:35815622..35815909hg19UCSC Ensembl
Outerchr20:35815555..35815949hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3557043
Supporting Variants
Samples
Known GenesRPN2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755790
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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