A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363927



Internal ID22589596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100506165..100509022hg38UCSC Ensembl
chr13:101158419..101161276hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg382858
hg192858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943372
Supporting Variants
Samples
Known GenesPCCA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363927
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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