A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454450



Internal ID22512326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:88549783..88556460hg38UCSC Ensembl
chr13:89202038..89208715hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg386678
hg196678
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863902
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454450
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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