A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8687889



Internal ID13343666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99833605..99836903hg38UCSC Ensembl
Innerchr10:99834605..99835903hg38UCSC Ensembl
Outerchr10:99832605..99837903hg38UCSC Ensembl
chr10:101593362..101596660hg19UCSC Ensembl
Innerchr10:101594362..101595660hg19UCSC Ensembl
Outerchr10:101592362..101597660hg19UCSC Ensembl
chr10:101583352..101586650hg18UCSC Ensembl
Innerchr10:101584352..101585650hg18UCSC Ensembl
Outerchr10:101582352..101587650hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg383299
hg193299
hg183299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3423829
Supporting Variants
SamplesNA12891
Known GenesABCC2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8687889
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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