A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620784



Internal ID6660965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77938944..77948509hg38UCSC Ensembl
Innerchr9:77938984..77948470hg38UCSC Ensembl
Outerchr9:77938905..77948549hg38UCSC Ensembl
chr9:80553860..80563425hg19UCSC Ensembl
Innerchr9:80553900..80563386hg19UCSC Ensembl
Outerchr9:80553821..80563465hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg389566
hg199566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1486e214
Supporting Variantsessv13532318
SamplesNA19338
Known GenesGNAQ
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620784
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer