A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457937



Internal ID22515818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:24996033..25006733hg38UCSC Ensembl
chr13:25570171..25580871hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3810701
hg1910701
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850393
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457937
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