A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868515



Internal ID22643450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44535034..44536439hg38UCSC Ensembl
chr22:44930914..44932319hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg381406
hg191406
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1408n209
Supporting Variantsnssv17484180, nssv17484181
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868515
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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