A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13622811



Internal ID3624628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128166528..128179690hg38UCSC Ensembl
Innerchr9:128166528..128179690hg38UCSC Ensembl
Outerchr9:128166028..128180190hg38UCSC Ensembl
chr9:130928807..130941969hg19UCSC Ensembl
Innerchr9:130928807..130941969hg19UCSC Ensembl
Outerchr9:130928307..130942469hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3813163
hg1913163
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621804
Supporting Variants
SamplesHG03234
Known GenesCIZ1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13622811
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