A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5584825



Internal ID8763631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54915508..54915836hg38UCSC Ensembl
chr6:54780306..54780634hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2678553
Supporting Variants
SamplesHG00154
Known GenesFAM83B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5584825
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