A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13526653



Internal ID1596940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75348480..75353831hg38UCSC Ensembl
Innerchr9:75348480..75353831hg38UCSC Ensembl
Outerchr9:75348132..75354133hg38UCSC Ensembl
chr9:77963396..77968747hg19UCSC Ensembl
Innerchr9:77963396..77968747hg19UCSC Ensembl
Outerchr9:77963048..77969049hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg385352
hg195352
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620719
Supporting Variants
SamplesHG01486
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13526653
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