A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13504905



Internal ID3506721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68432383..68585491hg38UCSC Ensembl
chr9:71047299..71200407hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38153109
hg19153109
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620544
Supporting Variants
SamplesHG03788
Known GenesLOC101927015, PGM5, TMEM252
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13504905
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