A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13546889



Internal ID2636057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86842993..86843364hg38UCSC Ensembl
Innerchr9:86842994..86843364hg38UCSC Ensembl
Outerchr9:86842993..86843365hg38UCSC Ensembl
chr9:89457908..89458279hg19UCSC Ensembl
Innerchr9:89457909..89458279hg19UCSC Ensembl
Outerchr9:89457908..89458280hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620967
Supporting Variants
SamplesHG02332
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13546889
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