A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3693e59



Internal ID22764913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160610630..160646928hg38UCSC Ensembl
chr6:161031662..161067960hg19UCSC Ensembl
chr6:160951652..160987950hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3836299
hg1936299
hg1836299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3413784, esv3413768, esv3325522
SamplesNA12891, NA12878, NA12892
Known GenesLPA
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3693e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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