A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18114044



Internal ID20681084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26288601..26294800hg38UCSC Ensembl
chr4:26290223..26296422hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374367
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18114044
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.03175


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