A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2722043



Internal ID5069333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:965414..965756hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv6839480, essv6832135, essv6921140, essv6925181
SamplesSSM083, SSM017, SSM018, SSM081
Known GenesRSPO4
Method
Analysis
PlatformIllumina HiSeq2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2722043
Frequency
Sample Size96
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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