A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7120469



Internal ID10052065
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 StatusS
Merged Variantsesv2850902
Supporting Variants
SamplesHuRef
Known GenesBCAR3
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7120469
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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