A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646872



Internal ID7033615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31883925..31887219hg38UCSC Ensembl
Innerchr21:31883975..31887169hg38UCSC Ensembl
Outerchr21:31883873..31887271hg38UCSC Ensembl
chr21:33256238..33259532hg19UCSC Ensembl
Innerchr21:33256288..33259482hg19UCSC Ensembl
Outerchr21:33256186..33259584hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg383295
hg193295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16312182
SamplesHG03297
Known GenesHUNK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646872
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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