A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7107469



Internal ID10039065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:10355791..10356140hg38UCSC Ensembl
Outerchr3:10397475..10397824hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2837902
Supporting Variants
SamplesHuRef
Known GenesATP2B2
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7107469
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