A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18109097



Internal ID20676137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:122918676..122919959hg38UCSC Ensembl
chr4:123839831..123841114hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg381284
hg191284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6385223
Supporting Variants
Samples
Known GenesNUDT6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18109097
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