A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621072



Internal ID6661253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91890704..91891812hg38UCSC Ensembl
Innerchr9:91890754..91891762hg38UCSC Ensembl
Outerchr9:91890594..91891922hg38UCSC Ensembl
chr9:94652986..94654094hg19UCSC Ensembl
Innerchr9:94653036..94654044hg19UCSC Ensembl
Outerchr9:94652876..94654204hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381109
hg191109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13559246
SamplesHG02878
Known GenesROR2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621072
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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