A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676503



Internal ID9942608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89962246..89967749hg38UCSC Ensembl
chr15:90505478..90510981hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg385504
hg195504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5906053, essv6101739, essv5694122, essv6553159, essv5659395
SamplesHG01170, NA19152, NA18523, NA18909, NA20348
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676503
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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