A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16957522



Internal ID38991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139103327..139103378hg38UCSC Ensembl
chr4:140024481..140024532hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457894
Supporting Variants
Samples
Known GenesELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16957522
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