A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661322



Internal ID9927427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124306124..124306304hg38UCSC Ensembl
chr10:125994693..125994873hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5778636, essv5969973, essv5565267, essv5599415, essv6359023, essv5893451, essv5760116, essv6123065, essv6414694
SamplesNA19393, NA19374, NA19373, NA19114, NA18523, NA19390, NA19108, NA19360, NA19398
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661322
Frequency
Sample Size1151
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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