A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5907965



Internal ID8885368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23768503..23850602hg38UCSC Ensembl
Outerchr20:23768469..23850637hg38UCSC Ensembl
Innerchr20:23749140..23831239hg19UCSC Ensembl
Outerchr20:23749106..23831274hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3882169
hg1982169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658403
Supporting Variants
SamplesNA18543
Known GenesCST2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5907965
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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