A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17414150



Internal ID22472020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:176450529..176450529hg38UCSC Ensembl
chr4:177371680..177371680hg19UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5954807
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17414150
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