A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6170696



Internal ID9035902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:49125709..49127882hg38UCSC Ensembl
Outerchr20:49125552..49128035hg38UCSC Ensembl
Innerchr20:47742246..47744419hg19UCSC Ensembl
Outerchr20:47742089..47744572hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg382484
hg192484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670489
Supporting Variants
SamplesHG00663
Known GenesSTAU1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6170696
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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