A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404637



Internal ID22462507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:22358261..22893783hg38UCSC Ensembl
chr22:22712609..23235963hg19UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38535523
hg19523355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5960481
Supporting Variants
Samples
Known GenesGGTLC2, IGLL5, LOC648691, MIR650, POM121L1P, PRAME, ZNF280A, ZNF280B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404637
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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