A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542948



Internal ID21867303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:27731333..27731333hg38UCSC Ensembl
chr4:27732955..27732955hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6071220
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542948
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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