A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949037



Internal ID22724495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160237516..160237516hg38UCSC Ensembl
chr3:159955303..159955303hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420786
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949037
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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