A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621990



Internal ID7008853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135428641..135465899hg38UCSC Ensembl
chr9:138320487..138357745hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3837259
hg1937259
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1515e214
Supporting Variantsessv13651990, essv13651991, essv13651989
SamplesHG01063, HG01259, HG00734
Known GenesPPP1R26-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621990
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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