A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659670



Internal ID9925775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31252714..31345081hg38UCSC Ensembl
Outerchr6:31252680..31345116hg38UCSC Ensembl
Innerchr6:31220491..31312858hg19UCSC Ensembl
Outerchr6:31220457..31312893hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3892437
hg1992437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1093e199
Supporting Variantsessv5898431
SamplesNA19725
Known GenesHLA-C
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659670
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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