A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13546874



Internal ID1264076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86832287..86839713hg38UCSC Ensembl
Innerchr9:86832316..86839685hg38UCSC Ensembl
Outerchr9:86832259..86839742hg38UCSC Ensembl
chr9:89447202..89454628hg19UCSC Ensembl
Innerchr9:89447231..89454600hg19UCSC Ensembl
Outerchr9:89447174..89454657hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg387427
hg197427
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620966
Supporting Variants
SamplesHG01111
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13546874
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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