A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17390015



Internal ID22447885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:22322968..22904988hg38UCSC Ensembl
chr22:22677324..23247168hg19UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38582021
hg19569845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5955656
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)nssv17390015
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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