A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13459067



Internal ID6669253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35118818..35124505hg38UCSC Ensembl
Innerchr9:35119318..35124005hg38UCSC Ensembl
Outerchr9:35117818..35125505hg38UCSC Ensembl
chr9:35118815..35124502hg19UCSC Ensembl
Innerchr9:35119315..35124002hg19UCSC Ensembl
Outerchr9:35117815..35125502hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg385688
hg195688
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620368
Supporting Variants
SamplesNA20809
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13459067
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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