A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5990909



Internal ID8968312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103396266..103398661hg38UCSC Ensembl
chr8:104408494..104410889hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg382396
hg192396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672690
Supporting Variants
SamplesNA18499
Known GenesSLC25A32
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5990909
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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