A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458360



Internal ID22516242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100506154..100509086hg38UCSC Ensembl
chr13:101158408..101161340hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg382933
hg192933
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863211
Supporting Variants
Samples
Known GenesPCCA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458360
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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