A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13407861



Internal ID3409677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15140390..15207671hg38UCSC Ensembl
chr9:15140388..15207669hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3867282
hg1967282
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619762
Supporting Variants
SamplesHG02139
Known GenesTTC39B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13407861
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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