A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5665614



Internal ID9710914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21361489..21366814hg38UCSC Ensembl
chr6:21361720..21367045hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg385326
hg195326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2668083
Supporting Variants
SamplesNA19463
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5665614
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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