A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621778



Internal ID6661954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127291852..127302271hg38UCSC Ensembl
Innerchr9:127291856..127302267hg38UCSC Ensembl
Outerchr9:127291848..127302275hg38UCSC Ensembl
chr9:130054131..130064550hg19UCSC Ensembl
Innerchr9:130054135..130064546hg19UCSC Ensembl
Outerchr9:130054127..130064554hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3810420
hg1910420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13621824
SamplesHG04222
Known GenesGARNL3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621778
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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