A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665821



Internal ID9585240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58166513..58173504hg38UCSC Ensembl
chr15:58458712..58465703hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg386992
hg196992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6141939, essv5508168, essv6383595
SamplesNA19664, NA19660, NA19685
Known GenesAQP9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665821
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer