A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204582



Internal ID20771622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33669006..33709521hg38UCSC Ensembl
chr22:34064992..34105507hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3840516
hg1940516
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553579
Supporting Variants
Samples
Known GenesLARGE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204582
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00059


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