A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1164e199



Internal ID20124466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158802909..158803665hg38UCSC Ensembl
chr6:159223941..159224697hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38757
hg19757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2677588, esv2668329
SamplesNA18867, HG00246, NA19380
Known GenesEZR
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1164e199
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