A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620786



Internal ID6660967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77982890..77984127hg38UCSC Ensembl
Innerchr9:77983063..77983954hg38UCSC Ensembl
Outerchr9:77982717..77984300hg38UCSC Ensembl
chr9:80597806..80599043hg19UCSC Ensembl
Innerchr9:80597979..80598870hg19UCSC Ensembl
Outerchr9:80597633..80599216hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg381238
hg191238
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13532320
SamplesHG02383
Known GenesGNAQ
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620786
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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