A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074892



Internal ID20641932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36901505..36908870hg38UCSC Ensembl
chr22:37297547..37304912hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg387366
hg197366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555004
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074892
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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