A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468403



Internal ID22526292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67368539..67381724hg38UCSC Ensembl
chr13:67942671..67955856hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3813186
hg1913186
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853715
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468403
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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