A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204640



Internal ID20771680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37904165..37911779hg38UCSC Ensembl
chr22:38300172..38307786hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg387615
hg197615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541586
Supporting Variants
Samples
Known GenesMICALL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204640
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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