A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943372



Internal ID22718820
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 StatusM
Merged Variants
Supporting Variantsnssv17363927
Samples
Known GenesPCCA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943372
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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