A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187220



Internal ID20754260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78331785..78334301hg38UCSC Ensembl
chr17:76327866..76330382hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382517
hg192517
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521298
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187220
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