A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388770



Internal ID22446640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112916193..112916193hg38UCSC Ensembl
chr13:113570507..113570507hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5969945
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388770
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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