A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2850902



Internal ID10523882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:93822819..93825703hg38UCSC Ensembl
Outerchr1:94288375..94291259hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg382885
hg192885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7120469
SamplesHuRef
Known GenesBCAR3
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2850902
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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