A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211237



Internal ID20778277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95728501..95758200hg38UCSC Ensembl
chr3:95447345..95477044hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3829700
hg1929700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356102
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211237
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00014


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