A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7128247



Internal ID10059843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:29711134..29711861hg38UCSC Ensembl
Outerchr10:30000063..30000790hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38728
hg19728
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2858680
Supporting Variants
SamplesHuRef
Known GenesSVIL
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7128247
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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