A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16956368



Internal ID38216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141709041..141709504hg38UCSC Ensembl
chr4:142630194..142630657hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469501
Supporting Variants
Samples
Known GenesIL15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16956368
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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