A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663264



Internal ID9582683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29893089..29947977hg38UCSC Ensembl
Outerchr6:29893055..29948012hg38UCSC Ensembl
Innerchr6:29860866..29915754hg19UCSC Ensembl
Outerchr6:29860832..29915789hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3854958
hg1954958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1087e199
Supporting Variantsessv5844316
SamplesHG00445
Known GenesHCG4B, HLA-A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663264
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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