A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13559402



Internal ID1885968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91968935..91976965hg38UCSC Ensembl
Innerchr9:91968935..91976965hg38UCSC Ensembl
Outerchr9:91968435..91977465hg38UCSC Ensembl
chr9:94731217..94739247hg19UCSC Ensembl
Innerchr9:94731217..94739247hg19UCSC Ensembl
Outerchr9:94730717..94739747hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg388031
hg198031
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621074
Supporting Variants
SamplesHG01776
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13559402
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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