A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033507



Internal ID21942850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30733833..30733912hg38UCSC Ensembl
chr13:31307970..31308049hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614625
Samples
Known GenesALOX5AP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033507
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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