A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13416360



Internal ID945870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20765066..20793859hg38UCSC Ensembl
Innerchr9:20765066..20793859hg38UCSC Ensembl
Outerchr9:20764566..20794359hg38UCSC Ensembl
chr9:20765065..20793858hg19UCSC Ensembl
Innerchr9:20765065..20793858hg19UCSC Ensembl
Outerchr9:20764565..20794358hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3828794
hg1928794
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619941
Supporting Variants
SamplesHG00580
Known GenesFOCAD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13416360
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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