A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3263829



Internal ID10936809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:26710147..26713284hg38UCSC Ensembl
Outerchr10:26999076..27002213hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383138
hg193138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7533396
SamplesHuRef
Known GenesPDSS1
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3263829
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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