A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565309



Internal ID7036691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:70377113..70385248hg38UCSC Ensembl
Outerchr10:72136869..72145004hg19UCSC Ensembl
Outerchr10:71806875..71815010hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg388136
hg198136
hg188136
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1000318
Supporting Variants
SamplesHuRef
Known GenesLRRC20
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565309
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