A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105803



Internal ID20672765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107585230..107586552hg38UCSC Ensembl
chr4:108506387..108507709hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg381323
hg191323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6393531
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105803
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