A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835279



Internal ID22610214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15123342..15124568hg38UCSC Ensembl
chr3:15164849..15166075hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg381227
hg191227
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485686
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835279
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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