A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097829



Internal ID20664869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182028284..182029337hg38UCSC Ensembl
chr3:181746072..181747125hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg381054
hg191054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369817
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097829
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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