A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16955601



Internal ID37707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109455745..109457687hg38UCSC Ensembl
chr4:110376901..110378843hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg381943
hg191943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472577
Supporting Variants
Samples
Known GenesSEC24B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16955601
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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