A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936276



Internal ID22711628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106775337..106775388hg38UCSC Ensembl
chr13:107427685..107427736hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351366
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936276
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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