A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960634



Internal ID22735606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186113324..186113324hg38UCSC Ensembl
chr3:185831113..185831113hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424476
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960634
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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