A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7734811



Internal ID13831814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46426766..46426767hg38UCSC Ensembl
Outerchr10:46426594..46426938hg38UCSC Ensembl
Innerchr10:47122988..47122989hg19UCSC Ensembl
Outerchr10:47122817..47123161hg19UCSC Ensembl
Innerchr10:46542995..46542994hg18UCSC Ensembl
Outerchr10:46542823..46543167hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38345
hg19345
hg18345
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302969
Supporting Variants
SamplesNA18572
Known GenesLINC00842
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7734811
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