A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18111536



Internal ID20678576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154718937..154719477hg38UCSC Ensembl
chr4:155640089..155640629hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6380096
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18111536
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00055


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