A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668414



Internal ID9934519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91811760..91812741hg38UCSC Ensembl
chr15:92354990..92355971hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38982
hg19982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6117968, essv5549553, essv5723375, essv5738208, essv6521493, essv6133344, essv6553827, essv6219125, essv5410862, essv6213106, essv6092180, essv5736306, essv5499045, essv5759269
SamplesNA19332, NA18917, NA18486, NA19377, NA19917, NA19371, NA19445, NA19462, NA18907, NA19461, NA19401, NA19440, NA19108, NA19473
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668414
Frequency
Sample Size1151
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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