A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17443554



Internal ID22501424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105666776..105666776hg38UCSC Ensembl
chr8:106679004..106679004hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5950472
Supporting Variants
Samples
Known GenesZFPM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17443554
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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