A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv139e199



Internal ID20123441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50422113..50430100hg38UCSC Ensembl
chr10:52181873..52189860hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg387988
hg197988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2670896, esv2669143
SamplesHG00476
Known GenesSGMS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv139e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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