A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294719



Internal ID20503937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34626310..34626387hg38UCSC Ensembl
chr22:35022302..35022379hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737220
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294719
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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