A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946773



Internal ID22722269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:70543391..70658161hg38UCSC Ensembl
chr13:71117523..71232293hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38114771
hg19114771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369660
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946773
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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