A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610962



Internal ID6651187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138741041..138754403hg38UCSC Ensembl
chr6:139062178..139075540hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3813363
hg1913363
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12565809, essv12565808
SamplesHG00148, NA20858
Known GenesLOC100507462
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610962
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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