A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543822



Internal ID20917063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:20041401..20075200hg38UCSC Ensembl
chr22:20028924..20062723hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3833800
hg1933800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072920
Samples
Known GenesTANGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543822
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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