A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927886



Internal ID22703119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77995146..78005443hg38UCSC Ensembl
chr13:78569281..78579578hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3810298
hg1910298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382330
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927886
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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