A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13546986



Internal ID2047521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86929779..86941227hg38UCSC Ensembl
Innerchr9:86929779..86941227hg38UCSC Ensembl
Outerchr9:86929279..86941727hg38UCSC Ensembl
chr9:89544694..89556142hg19UCSC Ensembl
Innerchr9:89544694..89556142hg19UCSC Ensembl
Outerchr9:89544194..89556642hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3811449
hg1911449
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620974
Supporting Variants
SamplesHG01871
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13546986
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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