A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1486e214



Internal ID20122909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77937978..77948805hg38UCSC Ensembl
chr9:80552894..80563721hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3810828
hg1910828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3620784, esv3620782
SamplesNA19338
Known GenesGNAQ
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1486e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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