A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13408034



Internal ID2418127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15255042..15337915hg38UCSC Ensembl
Innerchr9:15255042..15337915hg38UCSC Ensembl
Outerchr9:15254542..15338415hg38UCSC Ensembl
chr9:15255040..15337913hg19UCSC Ensembl
Innerchr9:15255040..15337913hg19UCSC Ensembl
Outerchr9:15254540..15338413hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3882874
hg1982874
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619774
Supporting Variants
SamplesHG02139
Known GenesTTC39B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13408034
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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