A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676084



Internal ID9595503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24864669..24874175hg38UCSC Ensembl
Outerchr15:24864298..24874545hg38UCSC Ensembl
Innerchr15:25109816..25119322hg19UCSC Ensembl
Outerchr15:25109445..25119692hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3810248
hg1910248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv444e199
Supporting Variantsessv6242641, essv6151919, essv6179585, essv5483167, essv5902395
SamplesNA19005, NA18973, NA19000, NA19072, NA19083
Known GenesSNRPN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676084
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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