A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5671062



Internal ID8648465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52766742..52769474hg38UCSC Ensembl
chr10:54526502..54529234hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg382733
hg192733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666698
Supporting Variants
SamplesNA19917
Known GenesMBL2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5671062
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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