A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459009



Internal ID22516891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18962725..18968777hg38UCSC Ensembl
chr13:19536865..19542917hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg386053
hg196053
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849899
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459009
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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