A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18116352



Internal ID20683392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41243299..41250217hg38UCSC Ensembl
chr4:41245316..41252234hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg386919
hg196919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6394336
Supporting Variants
Samples
Known GenesUCHL1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18116352
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