A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3695e59



Internal ID22764915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160634630..160646928hg38UCSC Ensembl
chr6:161055662..161067960hg19UCSC Ensembl
chr6:160975652..160987950hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3812299
hg1912299
hg1812299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3447523, esv3410664, esv3411642
SamplesNA19238, NA19239, NA19240
Known GenesLPA
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3695e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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