A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17641728



Internal ID21833775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43432794..43432794hg38UCSC Ensembl
chr22:43828734..43828734hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102578
Supporting Variants
Samples
Known GenesMPPED1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17641728
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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