A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191306



Internal ID20758346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32399553..32432607hg38UCSC Ensembl
chr17:30726572..30759626hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3833055
hg1933055
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513563
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191306
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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