A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8688063



Internal ID15009419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46557173..46586071hg38UCSC Ensembl
Innerchr10:46558173..46585071hg38UCSC Ensembl
Outerchr10:46556173..46587071hg38UCSC Ensembl
chr10:46963546..46992444hg19UCSC Ensembl
Innerchr10:46964546..46991444hg19UCSC Ensembl
Outerchr10:46962546..46993444hg19UCSC Ensembl
chr10:46383552..46412450hg18UCSC Ensembl
Innerchr10:46384552..46411450hg18UCSC Ensembl
Outerchr10:46382552..46413450hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3828899
hg1928899
hg1828899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3417603
Supporting Variants
SamplesNA19238
Known GenesSYT15
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8688063
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