A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13619350



Internal ID4338355
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621757
Supporting Variants
SamplesHG03882
Known GenesPBX3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13619350
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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