A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662215



Internal ID9581634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77939054..77948617hg38UCSC Ensembl
chr9:80553970..80563533hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg389564
hg199564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6101630
SamplesNA19338
Known GenesGNAQ
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662215
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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