A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13655167



Internal ID3058962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136213774..136236584hg38UCSC Ensembl
chr9:139105620..139128430hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3822811
hg1922811
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622003
Supporting Variants
SamplesHG02688
Known GenesQSOX2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13655167
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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