A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876924



Internal ID22651886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11332087..11338128hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg386042
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481002, nssv17481001
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876924
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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