A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5575113



Internal ID9546745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107492590..107494135hg38UCSC Ensembl
chr8:108504818..108506363hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg381546
hg191546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657528
Supporting Variants
SamplesNA19078
Known GenesANGPT1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5575113
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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