A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893893



Internal ID22668960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:91539551..91540061hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416601
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893893
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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