A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13569808



Internal ID5231325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94488449..94546593hg38UCSC Ensembl
Innerchr9:94488454..94546589hg38UCSC Ensembl
Outerchr9:94488445..94546598hg38UCSC Ensembl
chr9:97250731..97308875hg19UCSC Ensembl
Innerchr9:97250736..97308871hg19UCSC Ensembl
Outerchr9:97250727..97308880hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3858145
hg1958145
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621127
Supporting Variants
SamplesNA18626
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13569808
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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