A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099195



Internal ID20666235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4100085..4295563hg38UCSC Ensembl
chr3:4141769..4337247hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38195479
hg19195479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361824
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099195
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