A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204552



Internal ID20771592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19525953..19550222hg38UCSC Ensembl
chr22:19513476..19537745hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3824270
hg1924270
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552330
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204552
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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