A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074286



Internal ID20641326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34233359..34234058hg38UCSC Ensembl
chr22:34629348..34630047hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549845
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074286
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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