A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563707



Internal ID6688749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:62136144..62141567hg38UCSC Ensembl
Outerchr20:60711200..60716623hg19UCSC Ensembl
Outerchr20:60144595..60150018hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg385424
hg195424
hg185424
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1006840
Supporting Variants
SamplesHuRef
Known GenesPSMA7
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563707
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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