A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207990



Internal ID20775030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:161334993..162113020hg38UCSC Ensembl
chr3:161052781..161830808hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38778028
hg19778028
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362931
Supporting Variants
Samples
Known GenesLOC101243545, OTOL1, SPTSSB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207990
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