A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621757



Internal ID7008623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125940109..125945111hg38UCSC Ensembl
Innerchr9:125940109..125945111hg38UCSC Ensembl
Outerchr9:125939844..125945338hg38UCSC Ensembl
chr9:128702388..128707390hg19UCSC Ensembl
Innerchr9:128702388..128707390hg19UCSC Ensembl
Outerchr9:128702123..128707617hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385003
hg195003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13619350
SamplesHG03882
Known GenesPBX3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621757
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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