A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183440



Internal ID20750480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:83550927..83772145hg38UCSC Ensembl
chr13:84125062..84346280hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38221219
hg19221219
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6489261
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183440
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