A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6120120



Internal ID9097523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:20362772..20370678hg38UCSC Ensembl
Outerchr20:20362401..20371048hg38UCSC Ensembl
Innerchr20:20343416..20351322hg19UCSC Ensembl
Outerchr20:20343045..20351692hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg388648
hg198648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666074
Supporting Variants
SamplesNA19060
Known GenesINSM1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6120120
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer