A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880156



Internal ID22655126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27408890..27422972hg38UCSC Ensembl
chr22:27804851..27818933hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3814083
hg1914083
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482818
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880156
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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