A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13622826



Internal ID6092934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128429527..128434073hg38UCSC Ensembl
Innerchr9:128429531..128434070hg38UCSC Ensembl
Outerchr9:128429524..128434077hg38UCSC Ensembl
chr9:131191806..131196352hg19UCSC Ensembl
Innerchr9:131191810..131196349hg19UCSC Ensembl
Outerchr9:131191803..131196356hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg384547
hg194547
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621807
Supporting Variants
SamplesNA19472
Known GenesCERCAM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13622826
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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