A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406361



Internal ID22464231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:22343721..22893783hg38UCSC Ensembl
chr22:22698073..23235963hg19UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38550063
hg19537891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5955201
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)nssv17406361
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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