A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3302765



Internal ID15149713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24042870..24053230hg38UCSC Ensembl
Innerchr18:24042970..24053130hg38UCSC Ensembl
Outerchr18:24042770..24053330hg38UCSC Ensembl
chr18:21622834..21633194hg19UCSC Ensembl
Innerchr18:21622934..21633094hg19UCSC Ensembl
Outerchr18:21622734..21633294hg19UCSC Ensembl
chr18:19876832..19887192hg18UCSC Ensembl
Innerchr18:19876932..19887092hg18UCSC Ensembl
Outerchr18:19876732..19887292hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3810361
hg1910361
hg1810361
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7732262
SamplesNA18942
Known GenesTTC39C
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3302765
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer