A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2837902



Internal ID10510882
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 StatusM
Merged Variants
Supporting Variantsessv7107469
SamplesHuRef
Known GenesATP2B2
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2837902
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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