A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3297606



Internal ID10970586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:166083164..166083767hg38UCSC Ensembl
Outerchr4:167004316..167004919hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7567173
SamplesHuRef
Known GenesTLL1
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3297606
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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