A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13550391



Internal ID5753765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89684377..89690932hg38UCSC Ensembl
Innerchr9:89684404..89690906hg38UCSC Ensembl
Outerchr9:89684351..89690959hg38UCSC Ensembl
chr9:92299292..92305847hg19UCSC Ensembl
Innerchr9:92299319..92305821hg19UCSC Ensembl
Outerchr9:92299266..92305874hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg386556
hg196556
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621030
Supporting Variants
SamplesNA19121
Known GenesUNQ6494
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13550391
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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