A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672813



Internal ID9938918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32513905..32549643hg38UCSC Ensembl
Outerchr6:32513871..32549678hg38UCSC Ensembl
Innerchr6:32481682..32517420hg19UCSC Ensembl
Outerchr6:32481648..32517455hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3835808
hg1935808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1104e199
Supporting Variantsessv6158781
SamplesHG01259
Known GenesHLA-DRB5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672813
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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