A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660573



Internal ID9579992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24864195..24873614hg38UCSC Ensembl
chr15:25109342..25118761hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg389420
hg199420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv444e199
Supporting Variantsessv6065201, essv5784789
SamplesNA19000, NA19083
Known GenesSNRPN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660573
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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