A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610357



Internal ID6997274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110344206..110348941hg38UCSC Ensembl
chr6:110665409..110670144hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384736
hg194736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12502092, essv12502091
SamplesHG01896, NA19080
Known GenesMETTL24
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610357
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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