A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105796



Internal ID20672837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107538574..107539055hg38UCSC Ensembl
chr4:108459731..108460212hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392435
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105796
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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