A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669973



Internal ID9589392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29916361..30001871hg38UCSC Ensembl
chr6:29884138..29969648hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3885511
hg1985511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1088e199
Supporting Variantsessv5580976, essv5500616
SamplesHG00651, HG00662
Known GenesHCG4B, HCG9, HLA-A, ZNRD1-AS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669973
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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