A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5952138



Internal ID22727467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28844394..28844491hg38UCSC Ensembl
chr22:29240382..29240479hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398924
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5952138
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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