A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621764



Internal ID7008630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126258932..126270104hg38UCSC Ensembl
Innerchr9:126258932..126270104hg38UCSC Ensembl
Outerchr9:126258715..126270298hg38UCSC Ensembl
chr9:129021211..129032383hg19UCSC Ensembl
Innerchr9:129021211..129032383hg19UCSC Ensembl
Outerchr9:129020994..129032577hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3811173
hg1911173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13620856
SamplesHG02603
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621764
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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