A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18106309



Internal ID20673349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:113896901..113902100hg38UCSC Ensembl
chr4:114818057..114823256hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383106
Supporting Variants
Samples
Known GenesARSJ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18106309
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