A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469501



Internal ID247285
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 StatusM
Merged Variants
Supporting Variantsnssv16956368
Samples
Known GenesIL15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469501
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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