A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878663



Internal ID22653629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36389856..36398234hg38UCSC Ensembl
chr22:36785901..36794279hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg388379
hg198379
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482917
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878663
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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