A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5670921



Internal ID9895780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26611010..26617791hg38UCSC Ensembl
chr6:26611238..26618019hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg386782
hg196782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664019
Supporting Variants
SamplesNA20783
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5670921
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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