A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17491355



Internal ID22549280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184811370..184820404hg38UCSC Ensembl
chr4:185732524..185741558hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg389035
hg199035
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838810
Supporting Variants
Samples
Known GenesACSL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17491355
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