A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005389



Internal ID6717510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:166065984..166065984hg38UCSC Ensembl
chr4:166987136..166987136hg19UCSC Ensembl
chr4:167206586..167206586hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38129
hg19129
hg18129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3582247
SamplesHuRef
Known GenesTLL1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005389
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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