A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284003



Internal ID20493221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91244599..91244599hg38UCSC Ensembl
chr13:91896853..91896853hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754171
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284003
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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