A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105237



Internal ID20672277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78044545..78045037hg38UCSC Ensembl
chr3:78093696..78094188hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358432
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105237
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00064


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