A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17495488



Internal ID22553421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:134059777..134062949hg38UCSC Ensembl
chr5:133395468..133398640hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg383173
hg193173
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841134
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17495488
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