A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677483



Internal ID9596902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29003233..29003499hg38UCSC Ensembl
chr6:28971010..28971276hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6014731
SamplesHG01350
Known GenesZNF311
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677483
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