A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296506



Internal ID20505724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44904494..44904842hg38UCSC Ensembl
chr22:45300374..45300722hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740003
Supporting Variants
Samples
Known GenesPHF21B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296506
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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