A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5546863



Internal ID8524266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150006865..150070855hg38UCSC Ensembl
chr6:150328001..150391991hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3863991
hg1963991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678333
Supporting Variants
SamplesNA18546
Known GenesRAET1L, ULBP3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5546863
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