A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963300



Internal ID22738235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:16107394..16183588hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3876195
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397286
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963300
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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