A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453208



Internal ID22511082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:84220951..84225594hg38UCSC Ensembl
chr13:84795086..84799729hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg384644
hg194644
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5847775
Supporting Variants
Samples
Known GenesLINC00333
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453208
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