A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676927



Internal ID9596346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59193328..59193721hg38UCSC Ensembl
chr10:60953088..60953481hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38394
hg19394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5459724
SamplesNA18989
Known GenesPHYHIPL
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676927
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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