A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880885



Internal ID22655856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34553628..34557831hg38UCSC Ensembl
chr22:34949620..34953823hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg384204
hg194204
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482895
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880885
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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