A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13546997



Internal ID5866169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87060408..87068096hg38UCSC Ensembl
Innerchr9:87060408..87068096hg38UCSC Ensembl
Outerchr9:87060142..87068367hg38UCSC Ensembl
chr9:89675323..89683011hg19UCSC Ensembl
Innerchr9:89675323..89683011hg19UCSC Ensembl
Outerchr9:89675057..89683282hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg387689
hg197689
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620975
Supporting Variants
SamplesNA19247
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13546997
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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