A curated catalogue of human genomic structural variation




Variant Details

Variant: esv988231



Internal ID6724205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:76496426..76499135hg38UCSC Ensembl
Innerchr10:78256184..78258893hg19UCSC Ensembl
Innerchr10:77926190..77928899hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382710
hg192710
hg182710
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587218
SamplesHuRef
Known GenesC10orf11
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv988231
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer