A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17405281



Internal ID22463151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36145992..36195742hg38UCSC Ensembl
chr22:36542040..36591788hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3849751
hg1949749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961471
Supporting Variants
Samples
Known GenesAPOL3, APOL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17405281
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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