A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5872509



Internal ID8849913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110248533..110250682hg38UCSC Ensembl
chr6:110569736..110571885hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382150
hg192150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671329
Supporting Variants
SamplesHG00142
Known GenesMETTL24
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5872509
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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