A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183181



Internal ID20750221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105410438..105414585hg38UCSC Ensembl
chr13:106062787..106066934hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg384148
hg194148
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494173
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183181
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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