A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625323



Internal ID21573628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168793121..168793121hg38UCSC Ensembl
chr4:169714272..169714272hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124622, nssv17124863
SamplesHG00731, HG00732
Known GenesPALLD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625323
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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