A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664665



Internal ID9930770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:25661875..25662406hg38UCSC Ensembl
Outerchr21:25661838..25662456hg38UCSC Ensembl
Innerchr21:27034187..27034718hg19UCSC Ensembl
Outerchr21:27034150..27034768hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6120499, essv5576165
SamplesNA18486, NA19257
Known GenesJAM2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664665
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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