A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497024



Internal ID22554958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16293735..16295737hg38UCSC Ensembl
chr5:16293844..16295846hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg382003
hg192003
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842154
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497024
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