A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619834



Internal ID6660020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17244102..17247177hg38UCSC Ensembl
Innerchr9:17244113..17247166hg38UCSC Ensembl
Outerchr9:17244091..17247188hg38UCSC Ensembl
chr9:17244100..17247175hg19UCSC Ensembl
Innerchr9:17244111..17247164hg19UCSC Ensembl
Outerchr9:17244089..17247186hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg383076
hg193076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13411923
SamplesNA18979
Known GenesCNTLN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619834
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