A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620416



Internal ID7007287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38094788..38101716hg38UCSC Ensembl
Innerchr9:38094838..38101666hg38UCSC Ensembl
Outerchr9:38094709..38101795hg38UCSC Ensembl
chr9:38094785..38101713hg19UCSC Ensembl
Innerchr9:38094835..38101663hg19UCSC Ensembl
Outerchr9:38094706..38101792hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg386929
hg196929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13464434
SamplesHG01920
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620416
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