A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621144



Internal ID6661323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94954990..94956878hg38UCSC Ensembl
Innerchr9:94954996..94956873hg38UCSC Ensembl
Outerchr9:94954985..94956884hg38UCSC Ensembl
chr9:97717272..97719160hg19UCSC Ensembl
Innerchr9:97717278..97719155hg19UCSC Ensembl
Outerchr9:97717267..97719166hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg381889
hg191889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13571768
SamplesHG03754
Known GenesC9orf3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621144
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