A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671491



Internal ID9937596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31267169..31352239hg38UCSC Ensembl
Outerchr6:31267135..31352274hg38UCSC Ensembl
Innerchr6:31234946..31320016hg19UCSC Ensembl
Outerchr6:31234912..31320051hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3885140
hg1985140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1094e199
Supporting Variantsessv5936206, essv6590342
SamplesNA19117, NA19474
Known GenesHLA-C
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671491
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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