A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv444e199



Internal ID20123746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24864195..24874545hg38UCSC Ensembl
chr15:25109342..25119692hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3810351
hg1910351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2660573, esv2676084
SamplesNA19072, NA19083, NA18973, NA19000, NA19005
Known GenesSNRPN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv444e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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