A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5591039



Internal ID8568442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3181835..3181916hg38UCSC Ensembl
Outerchr1:3181782..3181991hg38UCSC Ensembl
Innerchr1:3098399..3098480hg19UCSC Ensembl
Outerchr1:3098346..3098555hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2657185
Supporting Variants
SamplesHG00344
Known GenesPRDM16
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5591039
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