A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958357



Internal ID22733428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40691990..40692092hg38UCSC Ensembl
chr22:41087994..41088096hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17400610
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958357
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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