A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13655169



Internal ID3058942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136246642..136274709hg38UCSC Ensembl
chr9:139138488..139166555hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3828068
hg1928068
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622005
Supporting Variants
SamplesHG02688
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13655169
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