A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869090



Internal ID22644026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29367081..29389016hg38UCSC Ensembl
chr22:29763070..29785005hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3821936
hg1921936
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482836
Samples
Known GenesAP1B1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869090
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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