A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646890



Internal ID7033632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32600176..32602281hg38UCSC Ensembl
Innerchr21:32600226..32602231hg38UCSC Ensembl
Outerchr21:32600108..32602349hg38UCSC Ensembl
chr21:33972486..33974591hg19UCSC Ensembl
Innerchr21:33972536..33974541hg19UCSC Ensembl
Outerchr21:33972418..33974659hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg382106
hg192106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16313524
SamplesHG04164
Known GenesC21orf59
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646890
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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