A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1369e199



Internal ID20124671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105745721..105786282hg38UCSC Ensembl
chr9:108508002..108548563hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3840562
hg1940562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2669689, esv2667207
SamplesHG00640, HG00311, HG00324, HG00336
Known GenesTMEM38B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1369e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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