A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541055



Internal ID20914341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:48082560..48135150hg38UCSC Ensembl
chr22:48478377..48530967hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg3852591
hg1952591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074075
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541055
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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