A curated catalogue of human genomic structural variation




Variant Details

Variant: esv991018



Internal ID7061679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167940471..167940528hg38UCSC Ensembl
chr6:168341151..168341208hg19UCSC Ensembl
chr6:168084000..168084057hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3858
hg1958
hg1858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3572160
SamplesHuRef
Known GenesMLLT4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv991018
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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