A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656634



Internal ID9922739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31282892..31362669hg38UCSC Ensembl
chr6:31250669..31330446hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3879778
hg1979778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1094e199
Supporting Variantsessv5593762
SamplesNA12341
Known GenesHLA-B, MIR6891
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656634
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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