A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621989



Internal ID7008852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135419296..135472035hg38UCSC Ensembl
Innerchr9:135419446..135471885hg38UCSC Ensembl
Outerchr9:135419146..135472185hg38UCSC Ensembl
chr9:138311142..138363881hg19UCSC Ensembl
Innerchr9:138311292..138363731hg19UCSC Ensembl
Outerchr9:138310992..138364031hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3852740
hg1952740
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1515e214
Supporting Variantsessv13651988, essv13651987, essv13651986
SamplesHG01063, HG01259, HG00734
Known GenesPPP1R26-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621989
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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