A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551070



Internal ID20924210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33204874..33215172hg38UCSC Ensembl
chr22:33600860..33611158hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3810299
hg1910299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073584
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551070
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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