A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465138



Internal ID22523027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:104583369..104586711hg38UCSC Ensembl
chr13:105235720..105239062hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg383343
hg193343
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855740
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465138
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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