A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645125



Internal ID21837172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50073026..50073026hg38UCSC Ensembl
chr22:50511455..50511455hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110422
Supporting Variants
Samples
Known GenesMLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645125
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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