A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620974



Internal ID7007844
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13546986, essv13546987
SamplesHG01871, NA18644
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620974
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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