A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102177



Internal ID20669217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37990021..37996235hg38UCSC Ensembl
chr3:38031512..38037726hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg386215
hg196215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357374
Supporting Variants
Samples
Known GenesVILL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102177
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