A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658161



Internal ID9577580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29929059..30009191hg38UCSC Ensembl
chr6:29896836..29976968hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3880133
hg1980133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1088e199
Supporting Variantsessv6021518
SamplesNA18564
Known GenesHCG9, HLA-A, HLA-J, ZNRD1-AS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658161
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