A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6381689



Internal ID8783502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24861885..24864274hg38UCSC Ensembl
chr15:25107032..25109421hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg382390
hg192390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666560
Supporting Variants
SamplesHG00186
Known GenesSNRPN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6381689
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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