A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998686



Internal ID6734618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1695051..1703932hg38UCSC Ensembl
Outerchr10:1737245..1746126hg19UCSC Ensembl
Outerchr10:1727245..1736126hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg388882
hg198882
hg188882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564335
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998686
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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