A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3425053



Internal ID15272010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19067312..19077910hg38UCSC Ensembl
Innerchr13:19068312..19076910hg38UCSC Ensembl
Outerchr13:19066312..19078910hg38UCSC Ensembl
chr13:19641452..19652050hg19UCSC Ensembl
Innerchr13:19642452..19651050hg19UCSC Ensembl
Outerchr13:19640452..19653050hg19UCSC Ensembl
chr13:18539452..18550050hg18UCSC Ensembl
Innerchr13:18540452..18549050hg18UCSC Ensembl
Outerchr13:18538452..18551050hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3810599
hg1910599
hg1810599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688877
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3425053
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