A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5990334



Internal ID9613028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68852253..68863920hg38UCSC Ensembl
chr10:70612009..70623676hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3811668
hg1911668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668546
Supporting Variants
SamplesNA19315
Known GenesSTOX1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5990334
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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