A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621071



Internal ID6661252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91801051..91803844hg38UCSC Ensembl
Innerchr9:91801051..91803844hg38UCSC Ensembl
Outerchr9:91800834..91804071hg38UCSC Ensembl
chr9:94563333..94566126hg19UCSC Ensembl
Innerchr9:94563333..94566126hg19UCSC Ensembl
Outerchr9:94563116..94566353hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg382794
hg192794
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13559245
SamplesNA19099
Known GenesROR2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621071
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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