A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955045



Internal ID22730267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173214599..173214599hg38UCSC Ensembl
chr3:172932389..172932389hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955045
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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