A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963646



Internal ID22738581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:16104210..16104266hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404585
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963646
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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