A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13518809



Internal ID3872595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73445676..73447956hg38UCSC Ensembl
Innerchr9:73445681..73447951hg38UCSC Ensembl
Outerchr9:73445671..73447961hg38UCSC Ensembl
chr9:76060592..76062872hg19UCSC Ensembl
Innerchr9:76060597..76062867hg19UCSC Ensembl
Outerchr9:76060587..76062877hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382281
hg192281
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620671
Supporting Variants
SamplesHG03515
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13518809
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer