A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17125403



Internal ID21448633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102598772..102598772hg38UCSC Ensembl
chr4:103519929..103519929hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5609677
Supporting Variants
SamplesHG00864
Known GenesNFKB1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17125403
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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