A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8687903



Internal ID14691909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124988593..124989691hg38UCSC Ensembl
Innerchr10:124988691..124989593hg38UCSC Ensembl
Outerchr10:124987593..124990691hg38UCSC Ensembl
chr10:126677162..126678260hg19UCSC Ensembl
Innerchr10:126677260..126678162hg19UCSC Ensembl
Outerchr10:126676162..126679260hg19UCSC Ensembl
chr10:126667152..126668250hg18UCSC Ensembl
Innerchr10:126668152..126667250hg18UCSC Ensembl
Outerchr10:126666152..126669250hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381099
hg191099
hg181099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3432429
Supporting Variants
SamplesNA19239
Known GenesCTBP2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8687903
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