A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563995



Internal ID6688378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:34651345..34656976hg38UCSC Ensembl
Outerchr20:33239149..33244780hg19UCSC Ensembl
Outerchr20:32702810..32708441hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg385632
hg195632
hg185632
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv989025
Supporting Variants
SamplesHuRef
Known GenesPIGU
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563995
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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