A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5822491



Internal ID9173482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487039..32540745hg38UCSC Ensembl
Outerchr6:32486468..32541115hg38UCSC Ensembl
Innerchr6:32454816..32508522hg19UCSC Ensembl
Outerchr6:32454245..32508892hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3854648
hg1954648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658503
Supporting Variants
SamplesHG01378
Known GenesHLA-DRB5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5822491
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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