A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286632



Internal ID20495850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29641693..29647714hg38UCSC Ensembl
chr13:30215830..30221851hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg386022
hg196022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740037
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286632
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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