A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621636



Internal ID7008504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:119529074..119542434hg38UCSC Ensembl
Innerchr9:119529074..119542434hg38UCSC Ensembl
Outerchr9:119528917..119542541hg38UCSC Ensembl
chr9:122291352..122304712hg19UCSC Ensembl
Innerchr9:122291352..122304712hg19UCSC Ensembl
Outerchr9:122291195..122304819hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3813361
hg1913361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13613194, essv13613197, essv13613196, essv13613195
SamplesNA18507, NA19198, NA18868, NA19108
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621636
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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