A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2010e59



Internal ID20128759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35296409..35299207hg38UCSC Ensembl
chr19:35787312..35790110hg19UCSC Ensembl
chr19:40479152..40481950hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg382799
hg192799
hg182799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3447618, esv3399211, esv3329030, esv3379757, esv3452034
SamplesNA19239, NA12892, NA19238, NA12878, NA19240
Known GenesMAG
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2010e59
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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