A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554010



Internal ID20927119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41624847..41625363hg38UCSC Ensembl
chr21:43045007..43045523hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071530
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554010
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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