A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646720



Internal ID7033463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25808293..25875235hg38UCSC Ensembl
Innerchr21:25808328..25875200hg38UCSC Ensembl
Outerchr21:25808258..25875270hg38UCSC Ensembl
chr21:27180604..27247546hg19UCSC Ensembl
Innerchr21:27180639..27247511hg19UCSC Ensembl
Outerchr21:27180569..27247581hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3866943
hg1966943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16297397
SamplesHG02512
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646720
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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