A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621725



Internal ID7008592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124788748..124793727hg38UCSC Ensembl
Innerchr9:124788782..124793693hg38UCSC Ensembl
Outerchr9:124788714..124793761hg38UCSC Ensembl
chr9:127551027..127556006hg19UCSC Ensembl
Innerchr9:127551061..127555972hg19UCSC Ensembl
Outerchr9:127550993..127556040hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg384980
hg194980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13618748
SamplesHG02275
Known GenesOLFML2A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621725
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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