A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101145



Internal ID20668185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25851906..25945523hg38UCSC Ensembl
chr3:25893397..25987014hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3893618
hg1993618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360346
Supporting Variants
Samples
Known GenesLINC00692
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101145
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