A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539190



Internal ID20912494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33974171..33981017hg38UCSC Ensembl
chr21:35346472..35353318hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg386847
hg196847
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072001
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539190
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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