A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094118



Internal ID20661158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127833744..127856419hg38UCSC Ensembl
chr3:127552587..127575262hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3822676
hg1922676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355903
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094118
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