A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670274



Internal ID9936379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12318668..12335798hg38UCSC Ensembl
chr16:12412525..12429655hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3817131
hg1917131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv481e199
Supporting Variantsessv5677522
SamplesHG00692
Known GenesSNX29
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670274
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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