A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838018



Internal ID22612953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14415771..14431642hg38UCSC Ensembl
chr4:14417395..14433266hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3815872
hg1915872
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499638
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838018
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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