A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6325333



Internal ID9584110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14741596..14741834hg38UCSC Ensembl
chr21:16113917..16114155hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2674389
Supporting Variants
SamplesNA19172
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6325333
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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