A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6460726



Internal ID8954567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11486143..11486334hg38UCSC Ensembl
chr16:11579999..11580190hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2668853
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6460726
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