A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668964



Internal ID2902051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:978863..979956hg38UCSC Ensembl
Outerchr20:978826..980006hg38UCSC Ensembl
Innerchr20:959506..960599hg19UCSC Ensembl
Outerchr20:959469..960649hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381181
hg191181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6003276
SamplesHG01183
Known GenesRSPO4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668964
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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