A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678423



Internal ID9944528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31272174..31357244hg38UCSC Ensembl
Outerchr6:31272140..31357279hg38UCSC Ensembl
Innerchr6:31239951..31325021hg19UCSC Ensembl
Outerchr6:31239917..31325056hg19UCSC 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 Variantsessv5699848
SamplesNA20755
Known GenesHLA-B, MIR6891
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678423
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer