A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540860



Internal ID20914148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25385518..25445398hg38UCSC Ensembl
chr21:26757831..26817710hg19UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg3859881
hg1959880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071636
Samples
Known GenesLINC00158
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540860
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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