A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276917



Internal ID20486135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44229100..44229305hg38UCSC Ensembl
chr22:44624980..44625185hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745564
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276917
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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