A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv165e199



Internal ID11592424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98735252..98749277hg38UCSC Ensembl
chr10:100495009..100509034hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3814026
hg1914026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2666325, esv2663153
SamplesHG01073
Known GenesHPSE2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv165e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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