A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5462180



Internal ID8439583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103310059..103311250hg38UCSC Ensembl
chr10:105069816..105071007hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg381192
hg191192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2664207
Supporting Variants
SamplesNA19428
Known GenesPCGF6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5462180
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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