A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5957133



Internal ID22732273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139874475..139874475hg38UCSC Ensembl
chr3:139593317..139593317hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17407263
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5957133
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer