A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664596



Internal ID9584015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15407848..15409093hg38UCSC Ensembl
chr16:15501705..15502950hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg381246
hg191246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5598072, essv6058188, essv6306562
SamplesNA19904, NA19443, NA19198
Known GenesMPV17L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664596
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