A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459676



Internal ID22517562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85268401..85272747hg38UCSC Ensembl
chr13:85842536..85846882hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg384347
hg194347
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861112
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459676
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