A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204639



Internal ID20771679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37772607..37786629hg38UCSC Ensembl
chr22:38168614..38182636hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3814023
hg1914023
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544156
Supporting Variants
Samples
Known GenesTRIOBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204639
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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