A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646933



Internal ID7033675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:35057786..35060649hg38UCSC Ensembl
Innerchr21:35057786..35060649hg38UCSC Ensembl
Outerchr21:35057703..35060727hg38UCSC Ensembl
chr21:36430083..36432946hg19UCSC Ensembl
Innerchr21:36430083..36432946hg19UCSC Ensembl
Outerchr21:36430000..36433024hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg382864
hg192864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16314937
SamplesNA19390
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646933
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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