A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876418



Internal ID22651379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17157904..17174194hg38UCSC Ensembl
chr22:17638794..17655084hg19UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg3816291
hg1916291
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489446
Samples
Known GenesCECR5, CECR5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876418
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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