A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620019



Internal ID7006892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23857391..23858168hg38UCSC Ensembl
Innerchr9:23857391..23858168hg38UCSC Ensembl
Outerchr9:23857336..23858225hg38UCSC Ensembl
chr9:23857389..23858166hg19UCSC Ensembl
Innerchr9:23857389..23858166hg19UCSC Ensembl
Outerchr9:23857334..23858223hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38778
hg19778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13431337, essv13431338
SamplesNA12842, HG03066
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620019
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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